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FDA 510(k)

BECKMAN B-4 TEB BUFFER KIT

K-Number: K791290 · 1979-08-03

ApplicantBeckman Instruments, Inc.
Decision Date1979-08-03
Product CodeJBD
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

BECKMAN B-4 TEB BUFFER KIT 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 1979-08-03 under 510(k) number K791290. The device is classified under product code JBD. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BECKMAN B-4 TEB BUFFER KIT?

BECKMAN B-4 TEB BUFFER KIT is a medical device that received FDA 510(k) clearance on 1979-08-03. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K791290.

When did BECKMAN B-4 TEB BUFFER KIT receive FDA 510(k) clearance?

BECKMAN B-4 TEB BUFFER KIT received FDA 510(k) clearance on 1979-08-03, under 510(k) number K791290.

Who is the listed applicant for BECKMAN B-4 TEB BUFFER KIT?

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 B-4 TEB BUFFER KIT?

The FDA product code for BECKMAN B-4 TEB BUFFER KIT is JBD.

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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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Related Devices (Code: JBD)

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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