KAPPLER PRO/VENT PROCEDURE GOWN
K-Number: K932694 · 1994-03-29
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Device Summary
Frequently Asked Questions
What is the KAPPLER PRO/VENT PROCEDURE GOWN?
KAPPLER PRO/VENT PROCEDURE GOWN is a medical device that received FDA 510(k) clearance on 1994-03-29. The listed applicant is Kappler, Inc.. The 510(k) number is K932694.
When did KAPPLER PRO/VENT PROCEDURE GOWN receive FDA 510(k) clearance?
KAPPLER PRO/VENT PROCEDURE GOWN received FDA 510(k) clearance on 1994-03-29, under 510(k) number K932694.
Who is the listed applicant for KAPPLER PRO/VENT PROCEDURE GOWN?
The FDA 510(k) record lists Kappler, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KAPPLER PRO/VENT PROCEDURE GOWN?
The FDA product code for KAPPLER PRO/VENT PROCEDURE GOWN is FYA.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Kappler, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: FYA)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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