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FDA 510(k)

SPECTROPHOTOMETER, MODEL 597 IR

K-Number: K770288 · 1977-03-10

Decision Date1977-03-10
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SPECTROPHOTOMETER, MODEL 597 IR is the device name listed in this FDA 510(k) record. The listed applicant is The Perkin-Elmer Corp.. It received FDA 510(k) clearance on 1977-03-10 under 510(k) number K770288. 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, MODEL 597 IR?

SPECTROPHOTOMETER, MODEL 597 IR is a medical device that received FDA 510(k) clearance on 1977-03-10. The listed applicant is The Perkin-Elmer Corp.. The 510(k) number is K770288.

When did SPECTROPHOTOMETER, MODEL 597 IR receive FDA 510(k) clearance?

SPECTROPHOTOMETER, MODEL 597 IR received FDA 510(k) clearance on 1977-03-10, under 510(k) number K770288.

Who is the listed applicant for SPECTROPHOTOMETER, MODEL 597 IR?

The FDA 510(k) record lists The Perkin-Elmer Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPECTROPHOTOMETER, MODEL 597 IR?

The FDA product code for SPECTROPHOTOMETER, MODEL 597 IR is JJQ.

Related Clinical Trials

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.

Other records listing The Perkin-Elmer Corp. as applicant

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.

View all 62 devices →

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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