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FDA 510(k)

IAFP THIOGLYCOLLATE W/O INDICATOR W/HEMIN&VITA. K1

K-Number: K872678 · 1987-08-07

ApplicantI.A.F. Production, Inc.
Decision Date1987-08-07
Product CodeKZI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

IAFP THIOGLYCOLLATE W/O INDICATOR W/HEMIN&VITA. K1 is the device name listed in this FDA 510(k) record. The listed applicant is I.A.F. Production, Inc.. It received FDA 510(k) clearance on 1987-08-07 under 510(k) number K872678. The device is classified under product code KZI. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IAFP THIOGLYCOLLATE W/O INDICATOR W/HEMIN&VITA. K1?

IAFP THIOGLYCOLLATE W/O INDICATOR W/HEMIN&VITA. K1 is a medical device that received FDA 510(k) clearance on 1987-08-07. The listed applicant is I.A.F. Production, Inc.. The 510(k) number is K872678.

When did IAFP THIOGLYCOLLATE W/O INDICATOR W/HEMIN&VITA. K1 receive FDA 510(k) clearance?

IAFP THIOGLYCOLLATE W/O INDICATOR W/HEMIN&VITA. K1 received FDA 510(k) clearance on 1987-08-07, under 510(k) number K872678.

Who is the listed applicant for IAFP THIOGLYCOLLATE W/O INDICATOR W/HEMIN&VITA. K1?

The FDA 510(k) record lists I.A.F. Production, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IAFP THIOGLYCOLLATE W/O INDICATOR W/HEMIN&VITA. K1?

The FDA product code for IAFP THIOGLYCOLLATE W/O INDICATOR W/HEMIN&VITA. K1 is KZI.

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Other records listing I.A.F. Production, Inc. as applicant

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Related Devices (Code: KZI)

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.

K884208LISTERIA SELECTIVE MEDIUM (OXFORD FORMULATION)Oxoid U.S.A., Inc.K881995DIAMOND'S MEDIUM MODIFIEDRemel Co.K880122MIDDLEBROOK 7H9 BROTHHardy MediaK880131LOWENSTEIN-JENSEN, GRUFTHardy MediaK880134MIDDLEBROOK 7H11 AGARHardy MediaK880138WALLENSTEIN MEDIUM SLANTHardy Media

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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