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FDA 510(k)

API 20E/UNISCEPT 20E

K-Number: K924814 · 1993-03-11

ApplicantAnalytical Products, Inc.
Decision Date1993-03-11
Product CodeJSS
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

API 20E/UNISCEPT 20E 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 1993-03-11 under 510(k) number K924814. The device is classified under product code JSS. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the API 20E/UNISCEPT 20E?

API 20E/UNISCEPT 20E is a medical device that received FDA 510(k) clearance on 1993-03-11. The listed applicant is Analytical Products, Inc.. The 510(k) number is K924814.

When did API 20E/UNISCEPT 20E receive FDA 510(k) clearance?

API 20E/UNISCEPT 20E received FDA 510(k) clearance on 1993-03-11, under 510(k) number K924814.

Who is the listed applicant for API 20E/UNISCEPT 20E?

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 20E/UNISCEPT 20E?

The FDA product code for API 20E/UNISCEPT 20E is JSS.

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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.

K923684API UNISCEPT MIC/TYPE 2 AND 3 AND MICRO MICK922926API UNISCEPT KB/TYPE 2 AND 3K901559MODIFICATION TO API UNISCEPT 20GPK901390DMAC INDOLE REAGENTK895796API UNISCEPT KBK884510MODIFICATION MICRO-MIC

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Related Devices (Code: JSS)

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.

K123418GRAM-NEGATIVE QUICKFISH BCAdvandx, Inc.K101558GNR TRAFFIC LIGHT PNA FISHAdvandx, Inc.K092236E.COLI/P. AERUGINOSA PNA FISHAdvandx, Inc.K092393EK/P. AERUGINOSA PNA FISHAdvandx, Inc.K082068E. COLI PNA FISHAdvandx, Inc.K081433EK/P. AERUGINOSA PNA FISHAdvandx, 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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