MEDIPACK SEE-THROUGH SEAL STERILIZATION POUCH— 510(k) K993764

Name: FDA 510(k) clearance K993764
Creator: U.S. Food and Drug Administration
Published: 1999-12-16

Substantially Equivalent

Medipack Medical Packaging Mfg. Co.

FDA 510(k) clearance K993764 for MEDIPACK SEE-THROUGH SEAL STERILIZATION POUCH, Substantially Equivalent on 1999-12-16. Applicant: Medipack Medical Packaging Mfg. Co.. Device class: 2.

Clearance details

Applicant: Medipack Medical Packaging Mfg. Co.
Product code: Code KCT
Device class: Class 2
Regulation: 21 CFR 880.6850
Advisory panel: General Hospital
Date received: 1999-11-08
Decision date: 1999-12-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Potomac, MD, US

Download summary PDF View on FDA.gov ↗

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