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FDA 510(k)

DELTA-LITE CASTING TAPE & SPLINTS

K-Number: K802522 · 1981-01-08

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1981-01-08
Product CodeFYH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DELTA-LITE CASTING TAPE & SPLINTS is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Professionals, Inc.. It received FDA 510(k) clearance on 1981-01-08 under 510(k) number K802522. The device is classified under product code FYH. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DELTA-LITE CASTING TAPE & SPLINTS?

DELTA-LITE CASTING TAPE & SPLINTS is a medical device that received FDA 510(k) clearance on 1981-01-08. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K802522.

When did DELTA-LITE CASTING TAPE & SPLINTS receive FDA 510(k) clearance?

DELTA-LITE CASTING TAPE & SPLINTS received FDA 510(k) clearance on 1981-01-08, under 510(k) number K802522.

Who is the listed applicant for DELTA-LITE CASTING TAPE & SPLINTS?

The FDA 510(k) record lists Johnson & Johnson Professionals, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DELTA-LITE CASTING TAPE & SPLINTS?

The FDA product code for DELTA-LITE CASTING TAPE & SPLINTS is FYH.

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Other records listing Johnson & Johnson Professionals, Inc. as applicant

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Related Devices (Code: FYH)

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.

K925145TRACE MODEL #'S 840, 841, 842, 845Trace Medical Equipment, Inc.K924984SPECIALIST(R) WALKERJohnson & Johnson Orthopaedics, Inc.K895092KUT-SHIELDKut-Guard, Inc.K852558SPLINTS(ALL TYPE)The Huxley Instrument Corp.K843400HYDRO-SPLINT A SPONGE-COMPRESS DRESSCompression Splint Products, Inc.K821693J & J DIP WATER ADDITIVEJohnson & Johnson Professionals, 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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