MULTIPLE PURPOSE FORCEPS
K-Number: K924792 · 1994-04-28
Advertisement
Device Summary
Frequently Asked Questions
What is the MULTIPLE PURPOSE FORCEPS?
MULTIPLE PURPOSE FORCEPS is a medical device that received FDA 510(k) clearance on 1994-04-28. The listed applicant is Nusurg, Inc.. The 510(k) number is K924792.
When did MULTIPLE PURPOSE FORCEPS receive FDA 510(k) clearance?
MULTIPLE PURPOSE FORCEPS received FDA 510(k) clearance on 1994-04-28, under 510(k) number K924792.
Who is the listed applicant for MULTIPLE PURPOSE FORCEPS?
The FDA 510(k) record lists Nusurg, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MULTIPLE PURPOSE FORCEPS?
The FDA product code for MULTIPLE PURPOSE FORCEPS is GCJ.
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 Nusurg, 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: GCJ)
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.
Advertisement