Prosthetic devices · 21 CFR 872 Subpart D
Polyvinyl Methylether Maleic Anhydride &/or Acid Copolymer & Carboxymethylce
Call for PMAs 12/26/96 per 61 FR 50707 on 9/27/96
- Companies listing it
- 00 makers
- Brands and models
- 0
- 510(k) clearances
- 00 in five years
- FDA name
- Polyvinyl Methylether Maleic Anhydride &/Or Acid Copolymer & Carboxymethylce
Official records: FDA product classification for KXY · 21 CFR 872.3500.
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026