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FDA 510(k)

DOWFLOW ALT-UV DETERMINATION

K-Number: K821536 · 1982-06-14

ApplicantThe Dow Chemical Co.
Decision Date1982-06-14
Product CodeCKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DOWFLOW ALT-UV DETERMINATION is the device name listed in this FDA 510(k) record. The listed applicant is The Dow Chemical Co.. It received FDA 510(k) clearance on 1982-06-14 under 510(k) number K821536. The device is classified under product code CKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DOWFLOW ALT-UV DETERMINATION?

DOWFLOW ALT-UV DETERMINATION is a medical device that received FDA 510(k) clearance on 1982-06-14. The listed applicant is The Dow Chemical Co.. The 510(k) number is K821536.

When did DOWFLOW ALT-UV DETERMINATION receive FDA 510(k) clearance?

DOWFLOW ALT-UV DETERMINATION received FDA 510(k) clearance on 1982-06-14, under 510(k) number K821536.

Who is the listed applicant for DOWFLOW ALT-UV DETERMINATION?

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

What is the FDA product code for DOWFLOW ALT-UV DETERMINATION?

The FDA product code for DOWFLOW ALT-UV DETERMINATION is CKA.

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Other records listing The Dow Chemical Co. 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.

K823474ENZYMATIC GLUCOSE DETERMINATIONK822154UREA NITROGEN (ENZYMATIC) DETERMINATIONK821315DOWFLOW ENZYMATIC TRIGLYCERIDES DETERMK820675BILIRUBIN(TOTAL) DETERMINATION CTMSK820714DOW BILIRUBIN(DIRECT) DETERMINATIONK812777DIRECT IRON REAGENT SET

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Related Devices (Code: CKA)

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.

K120945HITACHI CLINICAL ANALYZER S TEST REAGENT CARTRIDGE ALT, HITACHI CLINICAL ANALYZER S TEST REAGENT CARTRIDGE ASTHitachi Chemical Diagnostics, Inc.K113382ACE ALT REAGENTAlfa WassermannK061020DIMENSION VISTA ALBUMIN, ALKALINE PHOSPHATASE, ASPARTATE AMINO TRANSFERASE, CARBAMAZEPINE & ALANINE AMINO TRANSFERASEDade Behring, Inc.K020487CARESIDE ALTCareside, Inc.K980028ALT (GPT) LIQUID STABLE 2 VIAL - INCORPORATING DYNAMIC STABILIZATION TECHNOLOGY - (DST)Trace America, Inc.K973869TRACE REAGENT LINE FOR THE COBAS MIRATrace America, 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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