TAHOE SURGICAL INSTRUMENTS LIGATURE DEVICE
K-Number: K941944 · 1994-07-25
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Device Summary
Frequently Asked Questions
What is the TAHOE SURGICAL INSTRUMENTS LIGATURE DEVICE?
TAHOE SURGICAL INSTRUMENTS LIGATURE DEVICE is a medical device that received FDA 510(k) clearance on 1994-07-25. The listed applicant is Tahoe Surgical Instruments P.R., Inc.. The 510(k) number is K941944.
When did TAHOE SURGICAL INSTRUMENTS LIGATURE DEVICE receive FDA 510(k) clearance?
TAHOE SURGICAL INSTRUMENTS LIGATURE DEVICE received FDA 510(k) clearance on 1994-07-25, under 510(k) number K941944.
Who is the listed applicant for TAHOE SURGICAL INSTRUMENTS LIGATURE DEVICE?
The FDA 510(k) record lists Tahoe Surgical Instruments P.R., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TAHOE SURGICAL INSTRUMENTS LIGATURE DEVICE?
The FDA product code for TAHOE SURGICAL INSTRUMENTS LIGATURE DEVICE is HET.
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 Tahoe Surgical Instruments P.R., 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: HET)
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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