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FDA 510(k)

LUMINESCENCE PHOTOMETER 100 SERIES

K-Number: K810736 · 1981-03-31

Decision Date1981-03-31
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LUMINESCENCE PHOTOMETER 100 SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Sai Technology. It received FDA 510(k) clearance on 1981-03-31 under 510(k) number K810736. The device is classified under product code JJQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LUMINESCENCE PHOTOMETER 100 SERIES?

LUMINESCENCE PHOTOMETER 100 SERIES is a medical device that received FDA 510(k) clearance on 1981-03-31. The listed applicant is Sai Technology. The 510(k) number is K810736.

When did LUMINESCENCE PHOTOMETER 100 SERIES receive FDA 510(k) clearance?

LUMINESCENCE PHOTOMETER 100 SERIES received FDA 510(k) clearance on 1981-03-31, under 510(k) number K810736.

Who is the listed applicant for LUMINESCENCE PHOTOMETER 100 SERIES?

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

What is the FDA product code for LUMINESCENCE PHOTOMETER 100 SERIES?

The FDA product code for LUMINESCENCE PHOTOMETER 100 SERIES is JJQ.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: JJQ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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