FDA 510(k)

B-R-A-H-M-S PCT LIA

K-Number: K040887 · 2005-01-07

Decision Date2005-01-07

Product CodeNTM

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

B-R-A-H-M-S PCT LIA is the device name listed in this FDA 510(k) record. The listed applicant is Brahms Aktiengesellschaft. It received FDA 510(k) clearance on 2005-01-07 under 510(k) number K040887. The device is classified under product code NTM. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the B-R-A-H-M-S PCT LIA?

B-R-A-H-M-S PCT LIA is a medical device that received FDA 510(k) clearance on 2005-01-07. The listed applicant is Brahms Aktiengesellschaft. The 510(k) number is K040887.

When did B-R-A-H-M-S PCT LIA receive FDA 510(k) clearance?

B-R-A-H-M-S PCT LIA received FDA 510(k) clearance on 2005-01-07, under 510(k) number K040887.

Who is the listed applicant for B-R-A-H-M-S PCT LIA?

The FDA 510(k) record lists Brahms Aktiengesellschaft as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for B-R-A-H-M-S PCT LIA?

The FDA product code for B-R-A-H-M-S PCT LIA is NTM.

Other records listing Brahms Aktiengesellschaft 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.

K070310B R A H M S PCT SENSITIVE KRYPTOR TEST SYSTEM

Related Devices (Code: NTM)

K070310B R A H M S PCT SENSITIVE KRYPTOR TEST SYSTEMBrahms Aktiengesellschaft K071146VIDAS B.R.A.H.M.S. PCT ASSAYbioMerieux, Inc.

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.