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FDA 510(k)

MF 360B ELECTROSURGICAL UNIT

K-Number: K823923 · 1983-02-15

ApplicantAspen Laboratories, Inc.
Decision Date1983-02-15
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MF 360B ELECTROSURGICAL UNIT 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 1983-02-15 under 510(k) number K823923. 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 MF 360B ELECTROSURGICAL UNIT?

MF 360B ELECTROSURGICAL UNIT is a medical device that received FDA 510(k) clearance on 1983-02-15. The listed applicant is Aspen Laboratories, Inc.. The 510(k) number is K823923.

When did MF 360B ELECTROSURGICAL UNIT receive FDA 510(k) clearance?

MF 360B ELECTROSURGICAL UNIT received FDA 510(k) clearance on 1983-02-15, under 510(k) number K823923.

Who is the listed applicant for MF 360B ELECTROSURGICAL UNIT?

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 MF 360B ELECTROSURGICAL UNIT?

The FDA product code for MF 360B ELECTROSURGICAL UNIT is GEI.

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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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