DELTA-NET— 510(k) K790341

Name: FDA 510(k) clearance K790341
Creator: U.S. Food and Drug Administration
Published: 1979-04-04

Substantially Equivalent

Johnson & Johnson Professionals, Inc.

FDA 510(k) clearance K790341 for DELTA-NET, Substantially Equivalent on 1979-04-04. Applicant: Johnson & Johnson Professionals, Inc.. Device class: 2.

Clearance details

Applicant: Johnson & Johnson Professionals, Inc.
Product code: Code KKX
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 1979-02-21
Decision date: 1979-04-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Raynham, MA, US

Download summary PDF View on FDA.gov ↗

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