DRILL, CORDLESS SURGICAL— 510(k) K790063

Name: FDA 510(k) clearance K790063
Creator: U.S. Food and Drug Administration
Published: 1979-02-05

Substantially Equivalent

Richard'S Medical Equip., Inc.

FDA 510(k) clearance K790063 for DRILL, CORDLESS SURGICAL, Substantially Equivalent on 1979-02-05. Applicant: Richard'S Medical Equip., Inc.. Device class: 1.

Clearance details

Applicant: Richard'S Medical Equip., Inc.
Product code: Code KIJ
Device class: Class 1
Regulation: 21 CFR 878.4820
Advisory panel: General, Plastic Surgery
Date received: 1979-01-15
Decision date: 1979-02-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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