P.E.G. PATIENT CARE KIT
K-Number: K960177 · 1996-03-29
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Device Summary
Frequently Asked Questions
What is the P.E.G. PATIENT CARE KIT?
P.E.G. PATIENT CARE KIT is a medical device that received FDA 510(k) clearance on 1996-03-29. The listed applicant is United States Endoscopy Group, Inc.. The 510(k) number is K960177.
When did P.E.G. PATIENT CARE KIT receive FDA 510(k) clearance?
P.E.G. PATIENT CARE KIT received FDA 510(k) clearance on 1996-03-29, under 510(k) number K960177.
Who is the listed applicant for P.E.G. PATIENT CARE KIT?
The FDA 510(k) record lists United States Endoscopy Group, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for P.E.G. PATIENT CARE KIT?
The FDA product code for P.E.G. PATIENT CARE KIT is KNT.
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 United States Endoscopy Group, 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: KNT)
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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