INTROCULAR FLUID INJECTOR— 510(k) K881707

Name: FDA 510(k) clearance K881707
Creator: U.S. Food and Drug Administration
Published: 1988-10-21

Substantially Equivalent

B&B Medical Assoc., Inc.

FDA 510(k) clearance K881707 for INTROCULAR FLUID INJECTOR, Substantially Equivalent on 1988-10-21. Applicant: B&B Medical Assoc., Inc.. Device class: 2.

Clearance details

Applicant: B&B Medical Assoc., Inc.
Product code: Code FIH
Device class: Class 2
Regulation: 21 CFR 876.5820
Advisory panel: Gastroenterology, Urology
Date received: 1988-04-11
Decision date: 1988-10-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Danvers, MA, US

Download summary PDF View on FDA.gov ↗

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