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FDA 510(k)

AUTOMATED ELECTROPHORESES MACHINE

K-Number: K791111 · 1979-07-30

ApplicantGelman Sciences, Inc.
Decision Date1979-07-30
Product CodeJJN
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

AUTOMATED ELECTROPHORESES MACHINE is the device name listed in this FDA 510(k) record. The listed applicant is Gelman Sciences, Inc.. It received FDA 510(k) clearance on 1979-07-30 under 510(k) number K791111. The device is classified under product code JJN. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTOMATED ELECTROPHORESES MACHINE?

AUTOMATED ELECTROPHORESES MACHINE is a medical device that received FDA 510(k) clearance on 1979-07-30. The listed applicant is Gelman Sciences, Inc.. The 510(k) number is K791111.

When did AUTOMATED ELECTROPHORESES MACHINE receive FDA 510(k) clearance?

AUTOMATED ELECTROPHORESES MACHINE received FDA 510(k) clearance on 1979-07-30, under 510(k) number K791111.

Who is the listed applicant for AUTOMATED ELECTROPHORESES MACHINE?

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

What is the FDA product code for AUTOMATED ELECTROPHORESES MACHINE?

The FDA product code for AUTOMATED ELECTROPHORESES MACHINE is JJN.

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Other records listing Gelman Sciences, 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.

K946190DRUG DISPENSING SPIKEK943127PHARMASSURE LARGE VOLUME TRANSFER FILTERSK941589SYRINGE FILTER DEVICESK941020DRUG RECONSTITUTION FILTER DEVICEK942275VIAL VENT FILTERK941032UNKNOWN

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Related Devices (Code: JJN)

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.

K924021POWER SUPPLYThe Binding Site, Ltd.K924020ELECTROPHORESIS TANKThe Binding Site, Ltd.K882344ELECTR-TRANSBLOTTERThe W.E.P. Co.K881852REP SP ELECTROPHORESIS SYSTEM CAT NO. 3170Helena LaboratoriesK882163HELENA REP GEL PROCESSORHelena LaboratoriesK873352RAPID ELECTROPHORESIS SYSTEM (REP)Helena Laboratories

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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