CATHETER STRAP & RUINARY BAY HOLDER— 510(k) K780190

Name: FDA 510(k) clearance K780190
Creator: U.S. Food and Drug Administration
Published: 1978-02-21

Substantially Equivalent

Baka Manufacturing Co., Inc.

FDA 510(k) clearance K780190 for CATHETER STRAP & RUINARY BAY HOLDER, Substantially Equivalent on 1978-02-21. Applicant: Baka Manufacturing Co., Inc.. Device class: 1.

Clearance details

Applicant: Baka Manufacturing Co., Inc.
Product code: Code FAQ
Device class: Class 1
Regulation: 21 CFR 876.5250
Advisory panel: Gastroenterology, Urology
Date received: 1978-02-06
Decision date: 1978-02-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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