STERILIZATION PROCESS/T-BINDER— 510(k) K792629

Name: FDA 510(k) clearance K792629
Creator: U.S. Food and Drug Administration
Published: 1980-01-11

Substantially Equivalent

Procter & Gamble Mfg. Co.

FDA 510(k) clearance K792629 for STERILIZATION PROCESS/T-BINDER, Substantially Equivalent on 1980-01-11. Applicant: Procter & Gamble Mfg. Co.. Device class: 1.

Clearance details

Applicant: Procter & Gamble Mfg. Co.
Product code: Code KMO
Device class: Class 1
Regulation: 21 CFR 880.5160
Advisory panel: General Hospital
Date received: 1979-12-19
Decision date: 1980-01-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K861863 — MODIFIED PROTECTIVE GARMENT1986-08-11
K862348 — SINGLE-USE PATIENT UNDERPAD1986-07-02

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