← FDA Medical Device Classifications
Sheet, Recording, Breast Examination
NHM · Class II — Moderate Risk (510(k) clearance required) · Obstetrics/Gynecology · 21 CFR 884.2990
Classification
- FDA Product Code
NHM- Device class
- Class II — Moderate Risk (510(k) clearance required)
- Regulation
- 21 CFR 884.2990
- Review panel
- OB
- Medical specialty
- Obstetrics/Gynecology
- Submission type
- 4
- GMP exempt
- N
- Life sustaining
- N
- Implant
- N
- Third-party review
- N
Definition
This recording sheet is intended to for clinicians to mark the locationof a palpable breast lump identified by a clinical breast examination.
Market data
- Cleared 510(k) submissions
- 2
- Registered establishments
- 0
Source
- Authoritative
- FDA Device Classification database
- Machine
- JSON-LD · Markdown