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FDA 510(k)

DISP. ELECTROSURGERY PENCIL, HAND CONTROL

K-Number: K900633 · 1990-05-07

ApplicantMedical/Surgical Specialties, Ltd.
Decision Date1990-05-07
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DISP. ELECTROSURGERY PENCIL, HAND CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Medical/Surgical Specialties, Ltd.. It received FDA 510(k) clearance on 1990-05-07 under 510(k) number K900633. 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 DISP. ELECTROSURGERY PENCIL, HAND CONTROL?

DISP. ELECTROSURGERY PENCIL, HAND CONTROL is a medical device that received FDA 510(k) clearance on 1990-05-07. The listed applicant is Medical/Surgical Specialties, Ltd.. The 510(k) number is K900633.

When did DISP. ELECTROSURGERY PENCIL, HAND CONTROL receive FDA 510(k) clearance?

DISP. ELECTROSURGERY PENCIL, HAND CONTROL received FDA 510(k) clearance on 1990-05-07, under 510(k) number K900633.

Who is the listed applicant for DISP. ELECTROSURGERY PENCIL, HAND CONTROL?

The FDA 510(k) record lists Medical/Surgical Specialties, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISP. ELECTROSURGERY PENCIL, HAND CONTROL?

The FDA product code for DISP. ELECTROSURGERY PENCIL, HAND CONTROL is GEI.

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Other records listing Medical/Surgical Specialties, Ltd. 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: 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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