← FDA Medical Device Classifications

Disposable Joint Aspiration/Injection Kit

PPP · Class I — Low Risk (general controls) · General, Plastic Surgery · 21 CFR 878.4800

Classification

FDA Product Code
PPP
Device class
Class I — Low Risk (general controls)
Regulation
21 CFR 878.4800
Review panel
OR
Medical specialty
General, Plastic Surgery
Submission type
7
GMP exempt
N
Life sustaining
N
Implant
N
Third-party review
N

Definition

This product code has been established in accordance with the May 20, 1997, guidance entitled, convenience kits interim regulatory guidance, found at http://www.Fda.Gov/downloads/medicaldevices/deviceregulationandguidance/guidancedocuments/ucm080217.Pdf.This type of convenience kit, as listed in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market if it meets all criteria in the guidance.

Market data

Cleared 510(k) submissions
0
Registered establishments
7

Source

Authoritative
FDA Device Classification database
Machine
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