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FDA 510(k)

BUHLMANN VITAMIN B6 REA

K-Number: K955561 · 1996-05-23

ApplicantAmerican Laboratory Products Co., Ltd.
Decision Date1996-05-23
Product CodeCDD
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BUHLMANN VITAMIN B6 REA is the device name listed in this FDA 510(k) record. The listed applicant is American Laboratory Products Co., Ltd.. It received FDA 510(k) clearance on 1996-05-23 under 510(k) number K955561. The device is classified under product code CDD. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BUHLMANN VITAMIN B6 REA?

BUHLMANN VITAMIN B6 REA is a medical device that received FDA 510(k) clearance on 1996-05-23. The listed applicant is American Laboratory Products Co., Ltd.. The 510(k) number is K955561.

When did BUHLMANN VITAMIN B6 REA receive FDA 510(k) clearance?

BUHLMANN VITAMIN B6 REA received FDA 510(k) clearance on 1996-05-23, under 510(k) number K955561.

Who is the listed applicant for BUHLMANN VITAMIN B6 REA?

The FDA 510(k) record lists American Laboratory Products Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BUHLMANN VITAMIN B6 REA?

The FDA product code for BUHLMANN VITAMIN B6 REA is CDD.

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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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