PROVIEW SELF-SEALING STERILIZATION POUCH— 510(k) K893802

Name: FDA 510(k) clearance K893802
Creator: U.S. Food and Drug Administration
Published: 1990-04-04

Substantially Equivalent

Cottrell, Ltd.

FDA 510(k) clearance K893802 for PROVIEW SELF-SEALING STERILIZATION POUCH, Substantially Equivalent on 1990-04-04. Applicant: Cottrell, Ltd.. Device class: 2.

Clearance details

Applicant: Cottrell, Ltd.
Product code: Code KCT
Device class: Class 2
Regulation: 21 CFR 880.6850
Advisory panel: General Hospital
Date received: 1989-05-22
Decision date: 1990-04-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Englewood, CO, US

Download summary PDF View on FDA.gov ↗

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