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FDA 510(k)

SPECTROPHOTOMETER ANALYSIS SYS., AA-175

K-Number: K770443 · 1977-04-08

ApplicantVarian Assoc., Inc.
Decision Date1977-04-08
Product CodeJXR
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SPECTROPHOTOMETER ANALYSIS SYS., AA-175 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 1977-04-08 under 510(k) number K770443. The device is classified under product code JXR. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPECTROPHOTOMETER ANALYSIS SYS., AA-175?

SPECTROPHOTOMETER ANALYSIS SYS., AA-175 is a medical device that received FDA 510(k) clearance on 1977-04-08. The listed applicant is Varian Assoc., Inc.. The 510(k) number is K770443.

When did SPECTROPHOTOMETER ANALYSIS SYS., AA-175 receive FDA 510(k) clearance?

SPECTROPHOTOMETER ANALYSIS SYS., AA-175 received FDA 510(k) clearance on 1977-04-08, under 510(k) number K770443.

Who is the listed applicant for SPECTROPHOTOMETER ANALYSIS SYS., AA-175?

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 SPECTROPHOTOMETER ANALYSIS SYS., AA-175?

The FDA product code for SPECTROPHOTOMETER ANALYSIS SYS., AA-175 is JXR.

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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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