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FDA 510(k)

EXETRELUT

K-Number: K782066 · 1979-01-03

ApplicantMcb Manufacturing Chemists, Inc.
Decision Date1979-01-03
Product CodeKEA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

EXETRELUT is the device name listed in this FDA 510(k) record. The listed applicant is Mcb Manufacturing Chemists, Inc.. It received FDA 510(k) clearance on 1979-01-03 under 510(k) number K782066. The device is classified under product code KEA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXETRELUT?

EXETRELUT is a medical device that received FDA 510(k) clearance on 1979-01-03. The listed applicant is Mcb Manufacturing Chemists, Inc.. The 510(k) number is K782066.

When did EXETRELUT receive FDA 510(k) clearance?

EXETRELUT received FDA 510(k) clearance on 1979-01-03, under 510(k) number K782066.

Who is the listed applicant for EXETRELUT?

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

What is the FDA product code for EXETRELUT?

The FDA product code for EXETRELUT is KEA.

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.

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Other records listing Mcb Manufacturing Chemists, 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.

K801212WRIGHTS RAPID STAINK800847ENTELLANK792026WRIGHTS RAPID STAINK791929WRIGHTS RAPID STAIN

Related Devices (Code: KEA)

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.

K890997ZAVOS DISPOSABLE FILTRATION COLUMN (ZDFC)Atlantic Wholesale, Inc.K844948SYVA SOLID PHASE COLUMNSSyva Co.K842028CM-TRISACRYL M DEAE-TRISACRYL MLkb Instruments, Inc.K833320AMBERLITE CG50 RESIN, 100-200 MESHBiosan Laboratories, Inc.K833319BIO-REX 70 RESIN 100-200 MESH PH6.2Biosan Laboratories, Inc.K831027EXTRELUT QE EXTRACTION COLUMNSEmd Chemicals, Inc.

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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