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FDA 510(k)

INDIVIDUAL/LARGE/BELT FIRST AID KITS

K-Number: K914691 · 1992-01-15

ApplicantThe Lighthouse For the Blind, Inc.
Decision Date1992-01-15
Product CodeLYY
Advisory CommitteeHO
DecisionUnknown

Device Summary

INDIVIDUAL/LARGE/BELT FIRST AID KITS 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 1992-01-15 under 510(k) number K914691. The device is classified under product code LYY. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the INDIVIDUAL/LARGE/BELT FIRST AID KITS?

INDIVIDUAL/LARGE/BELT FIRST AID KITS is a medical device that received FDA 510(k) clearance on 1992-01-15. The listed applicant is The Lighthouse For the Blind, Inc.. The 510(k) number is K914691.

When did INDIVIDUAL/LARGE/BELT FIRST AID KITS receive FDA 510(k) clearance?

INDIVIDUAL/LARGE/BELT FIRST AID KITS received FDA 510(k) clearance on 1992-01-15, under 510(k) number K914691.

Who is the listed applicant for INDIVIDUAL/LARGE/BELT FIRST AID KITS?

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 INDIVIDUAL/LARGE/BELT FIRST AID KITS?

The FDA product code for INDIVIDUAL/LARGE/BELT FIRST AID KITS is LYY.

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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.

K941869SPLINT, PNEUMATIC, ARM & SPLINT, PNEUMATIC, LEG

Related Devices (Code: LYY)

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Official Source

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