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FDA 510(k)

SPECTROPHOTOMETERS,34,35,36,3600

K-Number: K770825 · 1977-07-11

Decision Date1977-07-11
Product Code
DecisionSubstantially Equivalent

Device Summary

SPECTROPHOTOMETERS,34,35,36,3600 is the device name listed in this FDA 510(k) record. The listed applicant is Beckman Instruments, Inc.. It received FDA 510(k) clearance on 1977-07-11 under 510(k) number K770825. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPECTROPHOTOMETERS,34,35,36,3600?

SPECTROPHOTOMETERS,34,35,36,3600 is a medical device that received FDA 510(k) clearance on 1977-07-11. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K770825.

When did SPECTROPHOTOMETERS,34,35,36,3600 receive FDA 510(k) clearance?

SPECTROPHOTOMETERS,34,35,36,3600 received FDA 510(k) clearance on 1977-07-11, under 510(k) number K770825.

Who is the listed applicant for SPECTROPHOTOMETERS,34,35,36,3600?

The FDA 510(k) record lists Beckman Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

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 Beckman Instruments, Inc. 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.

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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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