SUTURE REMOVAL KIT, STERILE, DISPOSABLE— 510(k) K920280

Name: FDA 510(k) clearance K920280
Creator: U.S. Food and Drug Administration
Published: 1992-05-11

Unknown

Trinity Laboratories, Inc.

FDA 510(k) clearance K920280 for SUTURE REMOVAL KIT, STERILE, DISPOSABLE, Unknown on 1992-05-11. Applicant: Trinity Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: Trinity Laboratories, Inc.
Product code: Code MCZ
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1992-01-22
Decision date: 1992-05-11
Decision: Unknown
Clearance type: Traditional
Location: Salisbury, MD, US

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