FDA 510(k)

MOIRE CONTOURGRAPH, MODELS MS-1, SS-1

K-Number: K790861 · 1979-05-07

Decision Date1979-05-07

Product Code

DecisionUnknown

Device Summary

MOIRE CONTOURGRAPH, MODELS MS-1, SS-1 is the device name listed in this FDA 510(k) record. The listed applicant is Otal Precision Co. , Ltd.. It received FDA 510(k) clearance on 1979-05-07 under 510(k) number K790861. FDA Decision: Unknown.

Frequently Asked Questions

What is the MOIRE CONTOURGRAPH, MODELS MS-1, SS-1?

MOIRE CONTOURGRAPH, MODELS MS-1, SS-1 is a medical device that received FDA 510(k) clearance on 1979-05-07. The listed applicant is Otal Precision Co. , Ltd.. The 510(k) number is K790861.

When did MOIRE CONTOURGRAPH, MODELS MS-1, SS-1 receive FDA 510(k) clearance?

MOIRE CONTOURGRAPH, MODELS MS-1, SS-1 received FDA 510(k) clearance on 1979-05-07, under 510(k) number K790861.

Who is the listed applicant for MOIRE CONTOURGRAPH, MODELS MS-1, SS-1?

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

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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.