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FDA 510(k)

SKATRON REPEATING DISPENSER

K-Number: K821034 · 1982-05-03

ApplicantSkatron, Inc.
Decision Date1982-05-03
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SKATRON REPEATING 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 1982-05-03 under 510(k) number K821034. The device is classified under product code JQW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SKATRON REPEATING DISPENSER?

SKATRON REPEATING DISPENSER is a medical device that received FDA 510(k) clearance on 1982-05-03. The listed applicant is Skatron, Inc.. The 510(k) number is K821034.

When did SKATRON REPEATING DISPENSER receive FDA 510(k) clearance?

SKATRON REPEATING DISPENSER received FDA 510(k) clearance on 1982-05-03, under 510(k) number K821034.

Who is the listed applicant for SKATRON REPEATING 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 SKATRON REPEATING DISPENSER?

The FDA product code for SKATRON REPEATING DISPENSER is JQW.

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.

K82196196 WELL DISPENSERK820992MICROPLATE WASHING DEVICEK812860IMMUNOASSAY PLATE

Related Devices (Code: JQW)

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.

K023955BD VIPER INSTRUMENTBecton, Dickinson & COK973335QUATRO SP SAMPLE PROCESSING SYSTEMS (200-499, INCLUSIVE)Zenyx Scientific , Ltd.K9801802700 SAMPLE MANAGERWaters CorporationK970420MASTERCAP AM 5.0/MASTERCAP RM 5.0Pharmacia, Inc.K970616MINI SAMPLER PROCESSORCavro Scientific Instruments, Inc.K962687GIO. DE VITA E C. S.R.L.(GDV) AUTOMATIC WASHING SYSTEMNichols Institute Diagnostics

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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