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FDA 510(k)

API UNISCEPT PLUS AUTOINOCULATOR

K-Number: K831341 · 1983-06-02

ApplicantAnalytical Products, Inc.
Decision Date1983-06-02
Product CodeJTC
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

API UNISCEPT PLUS AUTOINOCULATOR 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 1983-06-02 under 510(k) number K831341. The device is classified under product code JTC. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the API UNISCEPT PLUS AUTOINOCULATOR?

API UNISCEPT PLUS AUTOINOCULATOR is a medical device that received FDA 510(k) clearance on 1983-06-02. The listed applicant is Analytical Products, Inc.. The 510(k) number is K831341.

When did API UNISCEPT PLUS AUTOINOCULATOR receive FDA 510(k) clearance?

API UNISCEPT PLUS AUTOINOCULATOR received FDA 510(k) clearance on 1983-06-02, under 510(k) number K831341.

Who is the listed applicant for API UNISCEPT PLUS AUTOINOCULATOR?

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 UNISCEPT PLUS AUTOINOCULATOR?

The FDA product code for API UNISCEPT PLUS AUTOINOCULATOR is JTC.

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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.

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: JTC)

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.

K924907FILTERMATE UNIVERSAL HARVESTERPackard Instrument Co., Inc.K901808MICROMATE 196 MODEL A961960Packard Instrument Co., Inc.K894645IMMULON 1,2,3,AND 4 DIVIDASTRIPS TMDynatech Laboratories, Inc.K892369MULTI-PROBE HEAD PLUSHamilton Co.K891766GENETIC SYSTEMS MICROPLATE STRIP WASHERGenetic Systems Corp.K891765GENETIC SYSTEMS PIPETTOR/DILUTORGenetic Systems Corp.

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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