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FDA 510(k)

API 20A

K-Number: K771616 · 1977-09-02

ApplicantAnalytical Products, Inc.
Decision Date1977-09-02
Product CodeJSP
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

API 20A is the device name listed in this FDA 510(k) record. The listed applicant is Analytical Products, Inc.. It received FDA 510(k) clearance on 1977-09-02 under 510(k) number K771616. The device is classified under product code JSP. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the API 20A?

API 20A is a medical device that received FDA 510(k) clearance on 1977-09-02. The listed applicant is Analytical Products, Inc.. The 510(k) number is K771616.

When did API 20A receive FDA 510(k) clearance?

API 20A received FDA 510(k) clearance on 1977-09-02, under 510(k) number K771616.

Who is the listed applicant for API 20A?

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

What is the FDA product code for API 20A?

The FDA product code for API 20A is JSP.

Other records listing Analytical Products, 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.

K924814API 20E/UNISCEPT 20EK923684API UNISCEPT MIC/TYPE 2 AND 3 AND MICRO MICK922926API UNISCEPT KB/TYPE 2 AND 3K901559MODIFICATION TO API UNISCEPT 20GPK901390DMAC INDOLE REAGENTK895796API UNISCEPT KB

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Related Devices (Code: JSP)

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.

K945488LYFO(TM) DIFFERENTIAL DISKMicrobiologics, Inc.K945489LYFO(TM) DIFFERENTIAL DISKMicrobiologics, Inc.K945487LYFO(TM) DIFFERENTIAL DISKMicrobiologics, Inc.K944528BBLCRYSTAL ANAEROBE ID SYSTEMBecton Dickinson Microbiology SystemsK910666VITEK ANAEROBE IDENTIFICATION CARD, MODIFICATIONVitek Systems, Inc.K900996VITEK ANAEROBE IDENTIFICATION CARDVitek Systems, 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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