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FDA 510(k)

IIF-A-N-DNA TEST KIT

K-Number: K790106 · 1979-03-15

ApplicantMedica Corp.
Decision Date1979-03-15
Product CodeDHC
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

IIF-A-N-DNA TEST KIT is the device name listed in this FDA 510(k) record. The listed applicant is Medica Corp.. It received FDA 510(k) clearance on 1979-03-15 under 510(k) number K790106. The device is classified under product code DHC. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IIF-A-N-DNA TEST KIT?

IIF-A-N-DNA TEST KIT is a medical device that received FDA 510(k) clearance on 1979-03-15. The listed applicant is Medica Corp.. The 510(k) number is K790106.

When did IIF-A-N-DNA TEST KIT receive FDA 510(k) clearance?

IIF-A-N-DNA TEST KIT received FDA 510(k) clearance on 1979-03-15, under 510(k) number K790106.

Who is the listed applicant for IIF-A-N-DNA TEST KIT?

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

What is the FDA product code for IIF-A-N-DNA TEST KIT?

The FDA product code for IIF-A-N-DNA TEST KIT is DHC.

Other records listing Medica Corp. 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.

K123802EASYRA TBIL REAGENT, EASYRA DBII REAGENT, EASYRA CK REAGENTK120497EASYRA HBALC REGENT EASYCAL HBLC CALIBRATOR EASYQC HBALC MATERIALK111363PPX REAGENT, PPX CALIBRATORS, PPX QC MATERIALK111005ETHANOL REAGENT, ETHANOL CALIBRATOR, ETHANOL QC MATERIALK112788EASTLYTE NA/K/CA/PHK101089EASYRA MICRO-ALBUMIN REAGENT AND CALIBRATOR

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Related Devices (Code: DHC)

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.

K001352REAADS IGG ANTI-PROTHROMBIN SEMI-QUANTITATIVE TEST KITCorgenix, Inc.K001398REAADS IGM ANTI-PROTHROMBIN SEMI-QUANTITATIVE TEST KITCorgenix, Inc.K930247HUMAN A-DS DNA EIA KIT FOR DIAGNOSTIC USEThe Binding Site, Ltd.K930421ELIAS DSDNA ABSElias U.S.A., Inc.K914801IMMUNOWELL DSDNA ANTIBODY TESTGeneral Biometrics, Inc.K885048ACCESS R-CLONE ANA PROFILE ASSAYLipogen, 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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