GREENE-ARMYTAGE HEMOSTATIC FORCEPS
K-Number: K891397 · 1989-03-29
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Device Summary
Frequently Asked Questions
What is the GREENE-ARMYTAGE HEMOSTATIC FORCEPS?
GREENE-ARMYTAGE HEMOSTATIC FORCEPS is a medical device that received FDA 510(k) clearance on 1989-03-29. The listed applicant is Zinnanti Surgical Instruments, Inc.. The 510(k) number is K891397.
When did GREENE-ARMYTAGE HEMOSTATIC FORCEPS receive FDA 510(k) clearance?
GREENE-ARMYTAGE HEMOSTATIC FORCEPS received FDA 510(k) clearance on 1989-03-29, under 510(k) number K891397.
Who is the listed applicant for GREENE-ARMYTAGE HEMOSTATIC FORCEPS?
The FDA 510(k) record lists Zinnanti Surgical Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GREENE-ARMYTAGE HEMOSTATIC FORCEPS?
The FDA product code for GREENE-ARMYTAGE HEMOSTATIC FORCEPS is KNA.
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 Zinnanti Surgical Instruments, 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: KNA)
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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