ALLIGATOR CUP FORCEPS
K-Number: K772396 · 1978-01-17
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Device Summary
Frequently Asked Questions
What is the ALLIGATOR CUP FORCEPS?
ALLIGATOR CUP FORCEPS is a medical device that received FDA 510(k) clearance on 1978-01-17. The listed applicant is Edward Weck, Inc.. The 510(k) number is K772396.
When did ALLIGATOR CUP FORCEPS receive FDA 510(k) clearance?
ALLIGATOR CUP FORCEPS received FDA 510(k) clearance on 1978-01-17, under 510(k) number K772396.
Who is the listed applicant for ALLIGATOR CUP FORCEPS?
The FDA 510(k) record lists Edward Weck, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ALLIGATOR CUP FORCEPS?
The FDA product code for ALLIGATOR CUP FORCEPS is KAE.
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 Edward Weck, 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: KAE)
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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