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FDA 510(k)

MONEL 80&90 ULTRAVIOLET-VISIBLE SPEC.

K-Number: K800523 · 1980-03-20

ApplicantVarian Assoc., Inc.
Decision Date1980-03-20
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MONEL 80&90 ULTRAVIOLET-VISIBLE SPEC. is the device name listed in this FDA 510(k) record. The listed applicant is Varian Assoc., Inc.. It received FDA 510(k) clearance on 1980-03-20 under 510(k) number K800523. 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 MONEL 80&90 ULTRAVIOLET-VISIBLE SPEC.?

MONEL 80&90 ULTRAVIOLET-VISIBLE SPEC. is a medical device that received FDA 510(k) clearance on 1980-03-20. The listed applicant is Varian Assoc., Inc.. The 510(k) number is K800523.

When did MONEL 80&90 ULTRAVIOLET-VISIBLE SPEC. receive FDA 510(k) clearance?

MONEL 80&90 ULTRAVIOLET-VISIBLE SPEC. received FDA 510(k) clearance on 1980-03-20, under 510(k) number K800523.

Who is the listed applicant for MONEL 80&90 ULTRAVIOLET-VISIBLE SPEC.?

The FDA 510(k) record lists Varian Assoc., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MONEL 80&90 ULTRAVIOLET-VISIBLE SPEC.?

The FDA product code for MONEL 80&90 ULTRAVIOLET-VISIBLE SPEC. 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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