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FDA 510(k)

LDH PROCEDURE

K-Number: K781323 · 1978-08-31

ApplicantAnalytical & Research Chemicals, Inc.
Decision Date1978-08-31
Product Code
DecisionSubstantially Equivalent

Device Summary

LDH PROCEDURE is the device name listed in this FDA 510(k) record. The listed applicant is Analytical & Research Chemicals, Inc.. It received FDA 510(k) clearance on 1978-08-31 under 510(k) number K781323. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LDH PROCEDURE?

LDH PROCEDURE is a medical device that received FDA 510(k) clearance on 1978-08-31. The listed applicant is Analytical & Research Chemicals, Inc.. The 510(k) number is K781323.

When did LDH PROCEDURE receive FDA 510(k) clearance?

LDH PROCEDURE received FDA 510(k) clearance on 1978-08-31, under 510(k) number K781323.

Who is the listed applicant for LDH PROCEDURE?

The FDA 510(k) record lists Analytical & Research Chemicals, Inc. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing Analytical & Research Chemicals, 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.

K823784ENZYMATIC CHOLESTEROL (COLORIMETRICK823786ALKALINE PHOSPHATASEK823806DIRECT CREATININE PROCEDUREK781441BCG ALBUMIN REAGETK781460CHLORIDE REAGENTK781305UREA NITROGEN

View all 12 devices →

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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