# Medical Devices; Reclassification and Codification of Suction Lipoplasty System for Aesthetic Body Contouring
> **Food and Drug Administration** · Final rule. · Published 1998-02-17 · Effective 1998-03-19 · 63 FR 7703
## Document
- **Document number:** 98-3776
- **Category:** fda-device
- **Sub-agency:** Food and Drug Administration
- **Federal Register citation:** 63 FR 7703
- **CFR reference:** 21 CFR 878
- **Publication date:** 1998-02-17
- **Effective date:** 1998-03-19
- **HHS docket:** Docket No. 88P-0439
## Abstract

The Food and Drug Administration (FDA) is announcing that it has issued an order in the form of a letter to the American Society for Aesthetic Plastic Surgery (ASAPS) reclassifying the suction lipoplasty system for use in aesthetic body contouring from class III (premarket approval) to class II (special controls). The reclassification is based on information regarding the device contained in a reclassification petition submitted by ASAPS and other publicly available information. Accordingly, the order is being codified in the Code of Federal Regulations. This action is taken under the Medical Device Amendments of 1976 (the 1976 amendments) as amended by the Safe Medical Devices Act of 190 (the SMDA).

## Source
- [Federal Register document](https://www.federalregister.gov/documents/1998/02/17/98-3776/medical-devices-reclassification-and-codification-of-suction-lipoplasty-system-for-aesthetic-body)
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