MINOR SURGERY LIGHT

FDA 510(k) Premarket Notification · Submission K810207 · Applicant: Cavitron Corp.

Public Record 510(k) Submission Decision Date: 1981-02-13 510(k) record compiled from public FDA source records.

Submission Details & Decision

Normalized public record details for 510(k) notification K810207.

Source Dataset

FDA 510(k) Premarket Notifications

510(k) Number

K810207

Applicant / Sponsor

Cavitron Corp.

Device Name

MINOR SURGERY LIGHT

Product Code

GBC

Decision Date

1981-02-13

Decision / Status

Substantially Equivalent (SESE)

Advisory Committee

General, Plastic Surgery (SU)

Clearance Type

Traditional

Third Party Flag

Date Received

1981-01-26

Related Establishments / Registrations

JEDMED Instrument Company Registration: 1926681 View Registration

Public Record Disclaimer

This page represents an index of public-record FDA premarket notification filings. AvaSpecs is a private aggregator and is not affiliated with the FDA or any government agency. This page does not constitute medical, safety, legal, regulatory, or compliance advice. Information may be outdated or incomplete. Refer to official government source files for critical decisions.