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FDA 510(k)

BECKMAN DU-8 SPECTROPHOTOMETER

K-Number: K810511 · 1981-03-06

ApplicantBeckman Instruments, Inc.
Decision Date1981-03-06
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BECKMAN DU-8 SPECTROPHOTOMETER 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 1981-03-06 under 510(k) number K810511. 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 BECKMAN DU-8 SPECTROPHOTOMETER?

BECKMAN DU-8 SPECTROPHOTOMETER is a medical device that received FDA 510(k) clearance on 1981-03-06. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K810511.

When did BECKMAN DU-8 SPECTROPHOTOMETER receive FDA 510(k) clearance?

BECKMAN DU-8 SPECTROPHOTOMETER received FDA 510(k) clearance on 1981-03-06, under 510(k) number K810511.

Who is the listed applicant for BECKMAN DU-8 SPECTROPHOTOMETER?

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

What is the FDA product code for BECKMAN DU-8 SPECTROPHOTOMETER?

The FDA product code for BECKMAN DU-8 SPECTROPHOTOMETER is JJQ.

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Other records listing Beckman Instruments, 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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