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FDA 510(k)

SURFAS

K-Number: K925081 · 1993-09-28

ApplicantD.O. Weaver and Co.
Decision Date1993-09-28
Product CodeITX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SURFAS is the device name listed in this FDA 510(k) record. The listed applicant is D.O. Weaver and Co.. It received FDA 510(k) clearance on 1993-09-28 under 510(k) number K925081. The device is classified under product code ITX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURFAS?

SURFAS is a medical device that received FDA 510(k) clearance on 1993-09-28. The listed applicant is D.O. Weaver and Co.. The 510(k) number is K925081.

When did SURFAS receive FDA 510(k) clearance?

SURFAS received FDA 510(k) clearance on 1993-09-28, under 510(k) number K925081.

Who is the listed applicant for SURFAS?

The FDA 510(k) record lists D.O. Weaver and Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SURFAS?

The FDA product code for SURFAS is ITX.

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Related Devices (Code: ITX)

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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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