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FDA 510(k)

A.S.D. SAFETY TROCAR

K-Number: K955412 · 1996-05-14

ApplicantAmerican Surgical Devices
Decision Date1996-05-14
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

A.S.D. SAFETY TROCAR is the device name listed in this FDA 510(k) record. The listed applicant is American Surgical Devices. It received FDA 510(k) clearance on 1996-05-14 under 510(k) number K955412. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the A.S.D. SAFETY TROCAR?

A.S.D. SAFETY TROCAR is a medical device that received FDA 510(k) clearance on 1996-05-14. The listed applicant is American Surgical Devices. The 510(k) number is K955412.

When did A.S.D. SAFETY TROCAR receive FDA 510(k) clearance?

A.S.D. SAFETY TROCAR received FDA 510(k) clearance on 1996-05-14, under 510(k) number K955412.

Who is the listed applicant for A.S.D. SAFETY TROCAR?

The FDA 510(k) record lists American Surgical Devices as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for A.S.D. SAFETY TROCAR?

The FDA product code for A.S.D. SAFETY TROCAR is HET.

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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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