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FDA 510(k)

PR-3 ELISA TEST SYSTEM

K-Number: K961764 · 1996-08-19

ApplicantImmunoprobe, Inc.
Decision Date1996-08-19
Product CodeMOB
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

PR-3 ELISA TEST SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Immunoprobe, Inc.. It received FDA 510(k) clearance on 1996-08-19 under 510(k) number K961764. The device is classified under product code MOB. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PR-3 ELISA TEST SYSTEM?

PR-3 ELISA TEST SYSTEM is a medical device that received FDA 510(k) clearance on 1996-08-19. The listed applicant is Immunoprobe, Inc.. The 510(k) number is K961764.

When did PR-3 ELISA TEST SYSTEM receive FDA 510(k) clearance?

PR-3 ELISA TEST SYSTEM received FDA 510(k) clearance on 1996-08-19, under 510(k) number K961764.

Who is the listed applicant for PR-3 ELISA TEST SYSTEM?

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

What is the FDA product code for PR-3 ELISA TEST SYSTEM?

The FDA product code for PR-3 ELISA TEST SYSTEM is MOB.

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Other records listing Immunoprobe, 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.

K972406ADENOVIRUS ANTIGEN DETECTION ELISA TEST SYSTEMK971393MYCOPLASMA IGG ELISA TEST SYSTEMK961765MPO ELISA TEST SYSTEMK951549EBNA IGG EIA TEST SYSTEMK952521CARDIOLIPIN IGM EIA TEST SYSTEMK952522CARDIOLIPIN IGA EIA TEST SYSTEM

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Related Devices (Code: MOB)

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.

K261466Alegria Flash MPO; Alegria Flash PR3; Alegria Flash GBMZeus ScientificK243776Anti-Neutrophil Cytoplasmic Antibodies (Ethanol-Fixed); Anti-Neutrophil Cytoplasmic Antibodies (Formalin-Fixed)Zeus ScientificK172582EUROIMMUN IFA Granulocyte Mosaic™ EUROPattern and EUROIMMUN EUROPLUS Granulocyte Mosaic™ EUROPatternEuroimmun Us, Inc.K172461AESKUSLIDES ANCA Ethanol, AESKUSLIDES ANCA FormalinAesku.Diagnostics GmbH & Co. KGK173792EliA PR3s Immunoassay; EliA MPOs Immunoassay; EliA GBM ImmunoassayPhadia ABK161258NOVA Lite DAPI ANCA Ethanol Kit, NOVA Lite DAPI ANCA Formalin KitInova Diagnostics, 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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