CUPPED FORCEPS
K-Number: K833605 · 1984-01-03
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Device Summary
Frequently Asked Questions
What is the CUPPED FORCEPS?
CUPPED FORCEPS is a medical device that received FDA 510(k) clearance on 1984-01-03. The listed applicant is Microtek Medical, Inc.. The 510(k) number is K833605.
When did CUPPED FORCEPS receive FDA 510(k) clearance?
CUPPED FORCEPS received FDA 510(k) clearance on 1984-01-03, under 510(k) number K833605.
Who is the listed applicant for CUPPED FORCEPS?
The FDA 510(k) record lists Microtek Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CUPPED FORCEPS?
The FDA product code for CUPPED 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 Microtek Medical, 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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