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FDA 510(k)

KAB SYSTEM

K-Number: K951093 · 1995-03-24

ApplicantKing Systems Corp.
Decision Date1995-03-24
Product CodeBSF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

KAB SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is King Systems Corp.. It received FDA 510(k) clearance on 1995-03-24 under 510(k) number K951093. The device is classified under product code BSF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KAB SYSTEM?

KAB SYSTEM is a medical device that received FDA 510(k) clearance on 1995-03-24. The listed applicant is King Systems Corp.. The 510(k) number is K951093.

When did KAB SYSTEM receive FDA 510(k) clearance?

KAB SYSTEM received FDA 510(k) clearance on 1995-03-24, under 510(k) number K951093.

Who is the listed applicant for KAB SYSTEM?

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

What is the FDA product code for KAB SYSTEM?

The FDA product code for KAB SYSTEM is BSF.

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Other records listing King Systems 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.

K033189KING LTS REUSABLE OROPHARYNGEAL AIRWAY WITH DRAIN/SUCTION CHANNEL, MODELS KLT 303, KLT 304 AND KLT 305K033186KING LT-D DISPOSABLE OROPHARYNGEAL AIRWAY, MODELS KLT 203, KLT 204 AND KLT 205K021634KING LT, MODELS # KLT 100, KLT 101, KLT 102, KLT 103, KLT 104, KLT 105K012485MS-140 ALL-ROUND ENHANCED PERFORMANCE FILTER; MS-141 ALL-ROUND ENHANCED PERFORMANCE ANGLED; MS-142 ALL-ROUND/HME ENHANCEK010040SLEEVED FILTERK990614HME-BOOSTER

View all 18 devices →

Related Devices (Code: BSF)

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.

K852071OHMEDA GMS ABOSORBEROhmeda MedicalK843422OHMEDA BAIN CIRCUIT ADAPTER GMS ABSOROhmeda MedicalK834535NITROUS OXIDE RECYCLERG & L Unltd.K833452OHIO GMS ABSORBERAirco/Ohio Medical ProductsK821144OHIO ABSORBEROhio Medical ProductsK801255PENLON JUMBO CARBON DIOXIDE ABSORBERPenlon, 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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