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FDA 510(k)

CINEMEASURE (TM)

K-Number: K910654 · 1991-06-06

ApplicantSyracuse Research Corp.
Decision Date1991-06-06
Product CodeIZI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CINEMEASURE (TM) is the device name listed in this FDA 510(k) record. The listed applicant is Syracuse Research Corp.. It received FDA 510(k) clearance on 1991-06-06 under 510(k) number K910654. The device is classified under product code IZI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CINEMEASURE (TM)?

CINEMEASURE (TM) is a medical device that received FDA 510(k) clearance on 1991-06-06. The listed applicant is Syracuse Research Corp.. The 510(k) number is K910654.

When did CINEMEASURE (TM) receive FDA 510(k) clearance?

CINEMEASURE (TM) received FDA 510(k) clearance on 1991-06-06, under 510(k) number K910654.

Who is the listed applicant for CINEMEASURE (TM)?

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

What is the FDA product code for CINEMEASURE (TM)?

The FDA product code for CINEMEASURE (TM) is IZI.

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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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