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FDA 510(k)

SAFE-T-CLAMP

K-Number: K971277 · 1997-05-20

Decision Date1997-05-20
Product CodeKNA
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SAFE-T-CLAMP is the device name listed in this FDA 510(k) record. The listed applicant is Talon Medical, Ltd.. It received FDA 510(k) clearance on 1997-05-20 under 510(k) number K971277. The device is classified under product code KNA. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAFE-T-CLAMP?

SAFE-T-CLAMP is a medical device that received FDA 510(k) clearance on 1997-05-20. The listed applicant is Talon Medical, Ltd.. The 510(k) number is K971277.

When did SAFE-T-CLAMP receive FDA 510(k) clearance?

SAFE-T-CLAMP received FDA 510(k) clearance on 1997-05-20, under 510(k) number K971277.

Who is the listed applicant for SAFE-T-CLAMP?

The FDA 510(k) record lists Talon Medical, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SAFE-T-CLAMP?

The FDA product code for SAFE-T-CLAMP is KNA.

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.

Related Devices (Code: KNA)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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