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FDA 510(k)

SARTOPHOR SYSTEM FOR ELECTROPHORESIS

K-Number: K823132 · 1982-11-27

ApplicantSartorius Filters, Inc.
Decision Date1982-11-27
Product CodeJJN
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SARTOPHOR SYSTEM FOR ELECTROPHORESIS is the device name listed in this FDA 510(k) record. The listed applicant is Sartorius Filters, Inc.. It received FDA 510(k) clearance on 1982-11-27 under 510(k) number K823132. 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 SARTOPHOR SYSTEM FOR ELECTROPHORESIS?

SARTOPHOR SYSTEM FOR ELECTROPHORESIS is a medical device that received FDA 510(k) clearance on 1982-11-27. The listed applicant is Sartorius Filters, Inc.. The 510(k) number is K823132.

When did SARTOPHOR SYSTEM FOR ELECTROPHORESIS receive FDA 510(k) clearance?

SARTOPHOR SYSTEM FOR ELECTROPHORESIS received FDA 510(k) clearance on 1982-11-27, under 510(k) number K823132.

Who is the listed applicant for SARTOPHOR SYSTEM FOR ELECTROPHORESIS?

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

What is the FDA product code for SARTOPHOR SYSTEM FOR ELECTROPHORESIS?

The FDA product code for SARTOPHOR SYSTEM FOR ELECTROPHORESIS is JJN.

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Other records listing Sartorius Filters, 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.

K851816SARTORIUS MINISART FH 16534K851818SARTORIUS MINI SART FH 16592K851817SARTORIUS MINI-SART FH 16555K850435SARTORIUS AQUASART SM 40035 - DIALYSATE SYSK844504SARTORIUS MINISART SM 16596HYK830487HEMO-PROCESSING SYSTEM

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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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