Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MINOR SURGERY LIGHT

K-Number: K810207 · 1981-02-13

ApplicantCavitron Corp.
Decision Date1981-02-13
Product CodeGBC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MINOR SURGERY LIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Cavitron Corp.. It received FDA 510(k) clearance on 1981-02-13 under 510(k) number K810207. The device is classified under product code GBC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINOR SURGERY LIGHT?

MINOR SURGERY LIGHT is a medical device that received FDA 510(k) clearance on 1981-02-13. The listed applicant is Cavitron Corp.. The 510(k) number is K810207.

When did MINOR SURGERY LIGHT receive FDA 510(k) clearance?

MINOR SURGERY LIGHT received FDA 510(k) clearance on 1981-02-13, under 510(k) number K810207.

Who is the listed applicant for MINOR SURGERY LIGHT?

The FDA 510(k) record lists Cavitron Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MINOR SURGERY LIGHT?

The FDA product code for MINOR SURGERY LIGHT is GBC.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Cavitron Corp. 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.

K811582THE PLACERK802928SPIROMETRIC COMPUTER #SC-10K801623CAVITRON ULTRASONIC SURG. ASPIR. CUSAK801877SLIT LAMP ATTACHMENTK800869MODEL PM-20(N)(R)CO2 PATIENT MONITOR/ALAK800722AUTO-FIELD D AUTOMATED VISUAL DETECTOR

View all 32 devices →

Related Devices (Code: GBC)

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.

K896961HALUX EXLITE MINOR SURGERY LIGHTJedmed Instrument Co.K830610FLAT SUCTION DRAINSil-Med Corp.K811311SKYTRON ELITE SURGICAL TABLESSkytron, Div. the Kmw Group, Inc.

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.

↑