KUMAR T-ANCHORS HERNIA SET
K-Number: K081366 · 2008-07-15
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Device Summary
Frequently Asked Questions
What is the KUMAR T-ANCHORS HERNIA SET?
KUMAR T-ANCHORS HERNIA SET is a medical device that received FDA 510(k) clearance on 2008-07-15. The listed applicant is Nashville Surgical Instruments. The 510(k) number is K081366.
When did KUMAR T-ANCHORS HERNIA SET receive FDA 510(k) clearance?
KUMAR T-ANCHORS HERNIA SET received FDA 510(k) clearance on 2008-07-15, under 510(k) number K081366.
Who is the listed applicant for KUMAR T-ANCHORS HERNIA SET?
The FDA 510(k) record lists Nashville Surgical Instruments as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KUMAR T-ANCHORS HERNIA SET?
The FDA product code for KUMAR T-ANCHORS HERNIA SET is GAR.
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 Nashville Surgical Instruments 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: GAR)
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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