GENERAL PROCEDURE KIT
K-Number: K960248 · 1996-04-12
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Device Summary
Frequently Asked Questions
What is the GENERAL PROCEDURE KIT?
GENERAL PROCEDURE KIT is a medical device that received FDA 510(k) clearance on 1996-04-12. The listed applicant is Physician Industries, Inc.. The 510(k) number is K960248.
When did GENERAL PROCEDURE KIT receive FDA 510(k) clearance?
GENERAL PROCEDURE KIT received FDA 510(k) clearance on 1996-04-12, under 510(k) number K960248.
Who is the listed applicant for GENERAL PROCEDURE KIT?
The FDA 510(k) record lists Physician Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GENERAL PROCEDURE KIT?
The FDA product code for GENERAL PROCEDURE KIT is FMF.
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 Physician Industries, 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: FMF)
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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