BACTIDROP(TM) DOBELL & O'CONNOR IODINE— 510(k) K913006

Name: FDA 510(k) clearance K913006
Creator: U.S. Food and Drug Administration
Published: 1991-09-23

Substantially Equivalent

Remel Co.

FDA 510(k) clearance K913006 for BACTIDROP(TM) DOBELL & O'CONNOR IODINE, Substantially Equivalent on 1991-09-23. Applicant: Remel Co.. Device class: 1.

Clearance details

Applicant: Remel Co.
Product code: Code JTO
Device class: Class 1
Regulation: 21 CFR 866.2660
Advisory panel: Microbiology
Date received: 1991-07-08
Decision date: 1991-09-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lenexa, KS, US

Download summary PDF View on FDA.gov ↗

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