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FDA 510(k)

CARY 210 SERIES, SPECTROPHOTOMETER

K-Number: K791102 · 1979-07-17

ApplicantVarian Assoc., Inc.
Decision Date1979-07-17
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CARY 210 SERIES, SPECTROPHOTOMETER 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 1979-07-17 under 510(k) number K791102. 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 CARY 210 SERIES, SPECTROPHOTOMETER?

CARY 210 SERIES, SPECTROPHOTOMETER is a medical device that received FDA 510(k) clearance on 1979-07-17. The listed applicant is Varian Assoc., Inc.. The 510(k) number is K791102.

When did CARY 210 SERIES, SPECTROPHOTOMETER receive FDA 510(k) clearance?

CARY 210 SERIES, SPECTROPHOTOMETER received FDA 510(k) clearance on 1979-07-17, under 510(k) number K791102.

Who is the listed applicant for CARY 210 SERIES, SPECTROPHOTOMETER?

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 CARY 210 SERIES, SPECTROPHOTOMETER?

The FDA product code for CARY 210 SERIES, SPECTROPHOTOMETER 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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