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FDA 510(k)

SPLINT, PNEUMATIC, ARM & SPLINT, PNEUMATIC, LEG

K-Number: K941869 · 1994-08-03

ApplicantThe Lighthouse For the Blind, Inc.
Decision Date1994-08-03
Product CodeKZF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SPLINT, PNEUMATIC, ARM & SPLINT, PNEUMATIC, LEG is the device name listed in this FDA 510(k) record. The listed applicant is The Lighthouse For the Blind, Inc.. It received FDA 510(k) clearance on 1994-08-03 under 510(k) number K941869. The device is classified under product code KZF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPLINT, PNEUMATIC, ARM & SPLINT, PNEUMATIC, LEG?

SPLINT, PNEUMATIC, ARM & SPLINT, PNEUMATIC, LEG is a medical device that received FDA 510(k) clearance on 1994-08-03. The listed applicant is The Lighthouse For the Blind, Inc.. The 510(k) number is K941869.

When did SPLINT, PNEUMATIC, ARM & SPLINT, PNEUMATIC, LEG receive FDA 510(k) clearance?

SPLINT, PNEUMATIC, ARM & SPLINT, PNEUMATIC, LEG received FDA 510(k) clearance on 1994-08-03, under 510(k) number K941869.

Who is the listed applicant for SPLINT, PNEUMATIC, ARM & SPLINT, PNEUMATIC, LEG?

The FDA 510(k) record lists The Lighthouse For the Blind, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPLINT, PNEUMATIC, ARM & SPLINT, PNEUMATIC, LEG?

The FDA product code for SPLINT, PNEUMATIC, ARM & SPLINT, PNEUMATIC, LEG is KZF.

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.

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Other records listing The Lighthouse For the Blind, Inc. 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.

K914691INDIVIDUAL/LARGE/BELT FIRST AID KITS

Related Devices (Code: KZF)

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.

K954943NEVOSCOPENizar A. MullaniK952835WELCH ALLYN VIDEO EPISCOPEWelch Allyn, Inc.K945507H 5100, H 5200, H 5300Rudolf Riester GmbH & Co. KGK936088WAVE FLUORESCENT MAGNIFIERBurton Medical Products Corp.K940284MEDDEV MULTARRAY MEDICAL EXAMINING LIGHT MODIFICATIONMeddev International Corp.K933564SKYTRON EXAM LIGHTSkytron, Div. the Kmw Group, Inc.

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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