CHEMOSITE IMPLANTABLE DRUG DELIVERY— 510(k) K930632

Name: FDA 510(k) clearance K930632
Creator: U.S. Food and Drug Administration
Published: 1993-12-22

Substantially Equivalent

Device Labs, Inc.

FDA 510(k) clearance K930632 for CHEMOSITE IMPLANTABLE DRUG DELIVERY, Substantially Equivalent on 1993-12-22. Applicant: Device Labs, Inc.. Device class: 1.

Clearance details

Applicant: Device Labs, Inc.
Product code: Code KMF
Device class: Class 1
Regulation: 21 CFR 880.5090
Advisory panel: General Hospital
Date received: 1993-02-08
Decision date: 1993-12-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Medway, MA, US

Download summary PDF View on FDA.gov ↗

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