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FDA 510(k)

ASSERA-PLATE PROTEIN S KIT

K-Number: K870042 · 1987-02-13

ApplicantAmerican Bioproducts Co.
Decision Date1987-02-13
Product Code
DecisionSubstantially Equivalent

Device Summary

ASSERA-PLATE PROTEIN S KIT is the device name listed in this FDA 510(k) record. The listed applicant is American Bioproducts Co.. It received FDA 510(k) clearance on 1987-02-13 under 510(k) number K870042. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASSERA-PLATE PROTEIN S KIT?

ASSERA-PLATE PROTEIN S KIT is a medical device that received FDA 510(k) clearance on 1987-02-13. The listed applicant is American Bioproducts Co.. The 510(k) number is K870042.

When did ASSERA-PLATE PROTEIN S KIT receive FDA 510(k) clearance?

ASSERA-PLATE PROTEIN S KIT received FDA 510(k) clearance on 1987-02-13, under 510(k) number K870042.

Who is the listed applicant for ASSERA-PLATE PROTEIN S KIT?

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

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Other records listing American Bioproducts 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.

K983460STAR AUTOMATED MULTI-PARAMETRIC ANALYZERK971519ASSERACHROM TPA TEST KITK964716STA LIATEST CONTROL [N]+[P] KITK964728STA-LIATEST D-DI TEST KITK964718STA D-DI CALIBRATOR KITK962675STA - LIATEST VWF TEST KIT

View all 79 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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