STOMAHESIVE POWDER
K-Number: K792382 · 1979-12-20
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Device Summary
Frequently Asked Questions
What is the STOMAHESIVE POWDER?
STOMAHESIVE POWDER is a medical device that received FDA 510(k) clearance on 1979-12-20. The listed applicant is E. R. Squibb & Sons, Inc.. The 510(k) number is K792382.
When did STOMAHESIVE POWDER receive FDA 510(k) clearance?
STOMAHESIVE POWDER received FDA 510(k) clearance on 1979-12-20, under 510(k) number K792382.
Who is the listed applicant for STOMAHESIVE POWDER?
The FDA 510(k) record lists E. R. Squibb & Sons, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STOMAHESIVE POWDER?
The FDA product code for STOMAHESIVE POWDER is EXB.
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 E. R. Squibb & Sons, 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: EXB)
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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