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FDA 510(k)

ELECTROPHORESIS CONTROL LEVEL 1

K-Number: K925326 · 1993-03-26

ApplicantSeradyn, Inc.
Decision Date1993-03-26
Product CodeJJY
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ELECTROPHORESIS CONTROL LEVEL 1 is the device name listed in this FDA 510(k) record. The listed applicant is Seradyn, Inc.. It received FDA 510(k) clearance on 1993-03-26 under 510(k) number K925326. The device is classified under product code JJY. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTROPHORESIS CONTROL LEVEL 1?

ELECTROPHORESIS CONTROL LEVEL 1 is a medical device that received FDA 510(k) clearance on 1993-03-26. The listed applicant is Seradyn, Inc.. The 510(k) number is K925326.

When did ELECTROPHORESIS CONTROL LEVEL 1 receive FDA 510(k) clearance?

ELECTROPHORESIS CONTROL LEVEL 1 received FDA 510(k) clearance on 1993-03-26, under 510(k) number K925326.

Who is the listed applicant for ELECTROPHORESIS CONTROL LEVEL 1?

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

What is the FDA product code for ELECTROPHORESIS CONTROL LEVEL 1?

The FDA product code for ELECTROPHORESIS CONTROL LEVEL 1 is JJY.

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Other records listing Seradyn, Inc. as applicant

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Related Devices (Code: JJY)

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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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