MONOPOLAR ENDOSCOPIC REPOSABLE TIP SURGICAL INSTRUMENTS
K-Number: K943958 · 1994-09-07
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Device Summary
Frequently Asked Questions
What is the MONOPOLAR ENDOSCOPIC REPOSABLE TIP SURGICAL INSTRUMENTS?
MONOPOLAR ENDOSCOPIC REPOSABLE TIP SURGICAL INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1994-09-07. The listed applicant is Tnco, Inc.. The 510(k) number is K943958.
When did MONOPOLAR ENDOSCOPIC REPOSABLE TIP SURGICAL INSTRUMENTS receive FDA 510(k) clearance?
MONOPOLAR ENDOSCOPIC REPOSABLE TIP SURGICAL INSTRUMENTS received FDA 510(k) clearance on 1994-09-07, under 510(k) number K943958.
Who is the listed applicant for MONOPOLAR ENDOSCOPIC REPOSABLE TIP SURGICAL INSTRUMENTS?
The FDA 510(k) record lists Tnco, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MONOPOLAR ENDOSCOPIC REPOSABLE TIP SURGICAL INSTRUMENTS?
The FDA product code for MONOPOLAR ENDOSCOPIC REPOSABLE TIP SURGICAL INSTRUMENTS 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 Tnco, 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.
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