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FDA 510(k)

BENSON CCA100

K-Number: K924652 · 1993-04-09

ApplicantBenson Medical Instruments Co.
Decision Date1993-04-09
Product CodeEWG
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

BENSON CCA100 is the device name listed in this FDA 510(k) record. The listed applicant is Benson Medical Instruments Co.. It received FDA 510(k) clearance on 1993-04-09 under 510(k) number K924652. The device is classified under product code EWG. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BENSON CCA100?

BENSON CCA100 is a medical device that received FDA 510(k) clearance on 1993-04-09. The listed applicant is Benson Medical Instruments Co.. The 510(k) number is K924652.

When did BENSON CCA100 receive FDA 510(k) clearance?

BENSON CCA100 received FDA 510(k) clearance on 1993-04-09, under 510(k) number K924652.

Who is the listed applicant for BENSON CCA100?

The FDA 510(k) record lists Benson Medical Instruments Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BENSON CCA100?

The FDA product code for BENSON CCA100 is EWG.

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 Benson Medical Instruments Co. 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.

K123896CCS-200 SPIROMETERK982441CCA-220K981439CCA-200K963681CCA-100 (MODIFIED)

Related Devices (Code: EWG)

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.

K870587LASERMATIC SURGILASER MODEL 5050Lasermatic OYK880428ILLUMINA 25 CO2 LASER SYSTEMCooper Lasersonics, Inc.K880427ILLUMINA 40 CO2 LASER SYSTEMCooper Lasersonics, Inc.K880429ILLUMINA 55 CO2 LASER SYSTEMCooper Lasersonics, Inc.K872710MODEL 20-B W/OB-10A/U ATTACH. FOR EAR, NOSE/THROATDirected Energy, Inc.K870840MODEL 20-C W/BR-20A/U ATTACH/MODEL HL-3.O ATTACHDirected Energy, 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.

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