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FDA 510(k)

SANKEN MAT

K-Number: K924005 · 1993-06-17

ApplicantShima American Corp.
Decision Date1993-06-17
Product CodeFNM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SANKEN MAT is the device name listed in this FDA 510(k) record. The listed applicant is Shima American Corp.. It received FDA 510(k) clearance on 1993-06-17 under 510(k) number K924005. The device is classified under product code FNM. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SANKEN MAT?

SANKEN MAT is a medical device that received FDA 510(k) clearance on 1993-06-17. The listed applicant is Shima American Corp.. The 510(k) number is K924005.

When did SANKEN MAT receive FDA 510(k) clearance?

SANKEN MAT received FDA 510(k) clearance on 1993-06-17, under 510(k) number K924005.

Who is the listed applicant for SANKEN MAT?

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

What is the FDA product code for SANKEN MAT?

The FDA product code for SANKEN MAT is FNM.

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Related Devices (Code: FNM)

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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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