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FDA 510(k)

AGA UV PHOTOMETER

K-Number: K801499 · 1980-08-13

ApplicantSyva Co.
Decision Date1980-08-13
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

AGA UV PHOTOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Syva Co.. It received FDA 510(k) clearance on 1980-08-13 under 510(k) number K801499. 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 AGA UV PHOTOMETER?

AGA UV PHOTOMETER is a medical device that received FDA 510(k) clearance on 1980-08-13. The listed applicant is Syva Co.. The 510(k) number is K801499.

When did AGA UV PHOTOMETER receive FDA 510(k) clearance?

AGA UV PHOTOMETER received FDA 510(k) clearance on 1980-08-13, under 510(k) number K801499.

Who is the listed applicant for AGA UV PHOTOMETER?

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

What is the FDA product code for AGA UV PHOTOMETER?

The FDA product code for AGA UV PHOTOMETER is JJQ.

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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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