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FDA 510(k)

96 WELL DISPENSER

K-Number: K821961 · 1982-07-22

ApplicantSkatron, Inc.
Decision Date1982-07-22
Product CodeJTC
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

96 WELL DISPENSER is the device name listed in this FDA 510(k) record. The listed applicant is Skatron, Inc.. It received FDA 510(k) clearance on 1982-07-22 under 510(k) number K821961. 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 96 WELL DISPENSER?

96 WELL DISPENSER is a medical device that received FDA 510(k) clearance on 1982-07-22. The listed applicant is Skatron, Inc.. The 510(k) number is K821961.

When did 96 WELL DISPENSER receive FDA 510(k) clearance?

96 WELL DISPENSER received FDA 510(k) clearance on 1982-07-22, under 510(k) number K821961.

Who is the listed applicant for 96 WELL DISPENSER?

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

What is the FDA product code for 96 WELL DISPENSER?

The FDA product code for 96 WELL DISPENSER is JTC.

Related Clinical Trials

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.

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Other records listing Skatron, 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.

K821034SKATRON REPEATING DISPENSERK820992MICROPLATE WASHING DEVICEK812860IMMUNOASSAY PLATE

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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