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FDA 510(k)

SPECTROPHOTOMETER ANALYSIS SYSTEM

K-Number: K771637 · 1977-10-25

ApplicantVarian Assoc., Inc.
Decision Date1977-10-25
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SPECTROPHOTOMETER ANALYSIS SYSTEM 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 1977-10-25 under 510(k) number K771637. 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 SPECTROPHOTOMETER ANALYSIS SYSTEM?

SPECTROPHOTOMETER ANALYSIS SYSTEM is a medical device that received FDA 510(k) clearance on 1977-10-25. The listed applicant is Varian Assoc., Inc.. The 510(k) number is K771637.

When did SPECTROPHOTOMETER ANALYSIS SYSTEM receive FDA 510(k) clearance?

SPECTROPHOTOMETER ANALYSIS SYSTEM received FDA 510(k) clearance on 1977-10-25, under 510(k) number K771637.

Who is the listed applicant for SPECTROPHOTOMETER ANALYSIS SYSTEM?

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 SYSTEM?

The FDA product code for SPECTROPHOTOMETER ANALYSIS SYSTEM is JJQ.

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Other records listing Varian Assoc., Inc. as applicant

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Related Devices (Code: JJQ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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