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FDA 510(k)

ELECTROPHORESIS ACCESSORY MO. 3526

K-Number: K761248 · 1976-12-21

Decision Date1976-12-21
Product CodeJJN
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ELECTROPHORESIS ACCESSORY MO. 3526 is the device name listed in this FDA 510(k) record. The listed applicant is Gilford Instrument Laboratories, Inc.. It received FDA 510(k) clearance on 1976-12-21 under 510(k) number K761248. 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 ELECTROPHORESIS ACCESSORY MO. 3526?

ELECTROPHORESIS ACCESSORY MO. 3526 is a medical device that received FDA 510(k) clearance on 1976-12-21. The listed applicant is Gilford Instrument Laboratories, Inc.. The 510(k) number is K761248.

When did ELECTROPHORESIS ACCESSORY MO. 3526 receive FDA 510(k) clearance?

ELECTROPHORESIS ACCESSORY MO. 3526 received FDA 510(k) clearance on 1976-12-21, under 510(k) number K761248.

Who is the listed applicant for ELECTROPHORESIS ACCESSORY MO. 3526?

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

What is the FDA product code for ELECTROPHORESIS ACCESSORY MO. 3526?

The FDA product code for ELECTROPHORESIS ACCESSORY MO. 3526 is JJN.

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.

Other records listing Gilford Instrument Laboratories, 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.

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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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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