ATRAUMATIC TENACULA
K-Number: K891033 · 1989-03-17
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Device Summary
Frequently Asked Questions
What is the ATRAUMATIC TENACULA?
ATRAUMATIC TENACULA is a medical device that received FDA 510(k) clearance on 1989-03-17. The listed applicant is Zinnanti Surgical Instruments, Inc.. The 510(k) number is K891033.
When did ATRAUMATIC TENACULA receive FDA 510(k) clearance?
ATRAUMATIC TENACULA received FDA 510(k) clearance on 1989-03-17, under 510(k) number K891033.
Who is the listed applicant for ATRAUMATIC TENACULA?
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 ATRAUMATIC TENACULA?
The FDA product code for ATRAUMATIC TENACULA is HDC.
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: HDC)
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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