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FDA 510(k)

ELECTROSURGICAL DISPERSIVE PLATE

K-Number: K760675 · 1976-12-28

ApplicantAspen Laboratories, Inc.
Decision Date1976-12-28
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ELECTROSURGICAL DISPERSIVE PLATE is the device name listed in this FDA 510(k) record. The listed applicant is Aspen Laboratories, Inc.. It received FDA 510(k) clearance on 1976-12-28 under 510(k) number K760675. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTROSURGICAL DISPERSIVE PLATE?

ELECTROSURGICAL DISPERSIVE PLATE is a medical device that received FDA 510(k) clearance on 1976-12-28. The listed applicant is Aspen Laboratories, Inc.. The 510(k) number is K760675.

When did ELECTROSURGICAL DISPERSIVE PLATE receive FDA 510(k) clearance?

ELECTROSURGICAL DISPERSIVE PLATE received FDA 510(k) clearance on 1976-12-28, under 510(k) number K760675.

Who is the listed applicant for ELECTROSURGICAL DISPERSIVE PLATE?

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

What is the FDA product code for ELECTROSURGICAL DISPERSIVE PLATE?

The FDA product code for ELECTROSURGICAL DISPERSIVE PLATE is GEI.

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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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