TRI TALON RETRIEVAL FORCEPS
K-Number: K973071 · 1997-10-24
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Device Summary
Frequently Asked Questions
What is the TRI TALON RETRIEVAL FORCEPS?
TRI TALON RETRIEVAL FORCEPS is a medical device that received FDA 510(k) clearance on 1997-10-24. The listed applicant is Medical Engineering Laboratory, Inc.. The 510(k) number is K973071.
When did TRI TALON RETRIEVAL FORCEPS receive FDA 510(k) clearance?
TRI TALON RETRIEVAL FORCEPS received FDA 510(k) clearance on 1997-10-24, under 510(k) number K973071.
Who is the listed applicant for TRI TALON RETRIEVAL FORCEPS?
The FDA 510(k) record lists Medical Engineering Laboratory, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TRI TALON RETRIEVAL FORCEPS?
The FDA product code for TRI TALON RETRIEVAL FORCEPS is OCZ.
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 Medical Engineering Laboratory, 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: OCZ)
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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