FDA 510(k) clearance · back to tracker

ProGear® Surgical Mask with Oxafence®, Model AV82030

Prestige Ameritech cleared K231741 on 2024-09-05, decision: substantially equivalent

K-number

K231741

Sponsor

Prestige Ameritech

Device

ProGear® Surgical Mask with Oxafence®, Model AV82030

Class

Class II

Decision

Substantially Equivalent

Decision date

2024-09-05

Product code

OUK

Advisory committee

General, Plastic Surgery

Medical specialty

General, Plastic Surgery

Regulation number

878.4040

Official FDA record

Open K231741on accessdata.fda.gov →

FDA's authoritative 510(k) summary page. Includes the decision letter, predicate references, and downloadable substantial-equivalence determination.

openFDA JSON

Raw record →

Machine-readable JSON. Useful for cross-referencing classification, product code, and advisory committee fields.

Use this as a predicate

Drop K231741 into Compass and start a substantial-equivalence draft.

Compass pulls the predicate's intended use, technological characteristics, and performance data, maps them against your device, and produces a draft SE table aligned to FDA's 510(k) program guidance.

Try the sandbox

Source

Public 510(k) database, U.S. Food and Drug Administration, accessed via openFDA. Page refreshed weekly.