ANAL/RECTAL SYRINGE— 510(k) K761229

Name: FDA 510(k) clearance K761229
Creator: U.S. Food and Drug Administration
Published: 1977-02-24

Substantially Equivalent

Ace Orthopedic Manufacturing Co.

FDA 510(k) clearance K761229 for ANAL/RECTAL SYRINGE, Substantially Equivalent on 1977-02-24. Applicant: Ace Orthopedic Manufacturing Co.. Device class: 1.

Clearance details

Applicant: Ace Orthopedic Manufacturing Co.
Product code: Code KOA
Device class: Class 1
Regulation: 21 CFR 876.4730
Advisory panel: Gastroenterology, Urology
Date received: 1976-12-10
Decision date: 1977-02-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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