KAPPLER PRO/VENT BOOT— 510(k) K932738

Substantially Equivalent

Kappler, Inc.

FDA 510(k) clearance K932738 for KAPPLER PRO/VENT BOOT, Substantially Equivalent on 1994-03-29. Applicant: Kappler, Inc.. Device class: 1.

Clearance details

Applicant: Kappler, Inc.
Product code: Code FXP
Device class: Class 1
Regulation: 21 CFR 878.4040
Advisory panel: General, Plastic Surgery
Date received: 1993-06-07
Decision date: 1994-03-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Guntersville, AL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Kappler, Inc.

K932694 — KAPPLER PRO/VENT PROCEDURE GOWN1994-03-29

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