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FDA 510(k)

MODEL DMS 100 ULTRAVIOLET-VISIBLE SPEC

K-Number: K831866 · 1983-07-28

ApplicantVarian Assoc., Inc.
Decision Date1983-07-28
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MODEL DMS 100 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 1983-07-28 under 510(k) number K831866. 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 MODEL DMS 100 ULTRAVIOLET-VISIBLE SPEC?

MODEL DMS 100 ULTRAVIOLET-VISIBLE SPEC is a medical device that received FDA 510(k) clearance on 1983-07-28. The listed applicant is Varian Assoc., Inc.. The 510(k) number is K831866.

When did MODEL DMS 100 ULTRAVIOLET-VISIBLE SPEC receive FDA 510(k) clearance?

MODEL DMS 100 ULTRAVIOLET-VISIBLE SPEC received FDA 510(k) clearance on 1983-07-28, under 510(k) number K831866.

Who is the listed applicant for MODEL DMS 100 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 MODEL DMS 100 ULTRAVIOLET-VISIBLE SPEC?

The FDA product code for MODEL DMS 100 ULTRAVIOLET-VISIBLE SPEC is JJQ.

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Related Devices (Code: 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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