NEEDLE-GRABBER— 510(k) K923840

Substantially Equivalent

Guardian Angel Products, Inc.

FDA 510(k) clearance K923840 for NEEDLE-GRABBER, Substantially Equivalent on 1993-07-13. Applicant: Guardian Angel Products, Inc.. Device class: 1.

Clearance details

Applicant
Guardian Angel Products, Inc.
Product code
Code GDF
Device class
Class 1
Regulation
21 CFR 878.4800
Advisory panel
General, Plastic Surgery
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Washington, DC, US
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