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FDA 510(k)

URIAS PRESSURE SPLINTS, & FIRST AID

K-Number: K831764 · 1983-09-12

ApplicantSvenol Andersen
Decision Date1983-09-12
Product CodeFZF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

URIAS PRESSURE SPLINTS, & FIRST AID is the device name listed in this FDA 510(k) record. The listed applicant is Svenol Andersen. It received FDA 510(k) clearance on 1983-09-12 under 510(k) number K831764. The device is classified under product code FZF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the URIAS PRESSURE SPLINTS, & FIRST AID?

URIAS PRESSURE SPLINTS, & FIRST AID is a medical device that received FDA 510(k) clearance on 1983-09-12. The listed applicant is Svenol Andersen. The 510(k) number is K831764.

When did URIAS PRESSURE SPLINTS, & FIRST AID receive FDA 510(k) clearance?

URIAS PRESSURE SPLINTS, & FIRST AID received FDA 510(k) clearance on 1983-09-12, under 510(k) number K831764.

Who is the listed applicant for URIAS PRESSURE SPLINTS, & FIRST AID?

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

What is the FDA product code for URIAS PRESSURE SPLINTS, & FIRST AID?

The FDA product code for URIAS PRESSURE SPLINTS, & FIRST AID is FZF.

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Related Devices (Code: FZF)

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.

K881516COMPRESAIDR. Evans Corp.K874051INFLATABLE FULL LEG SPLINTVinyl Technology, Inc.K874052INFLATABLE HALF LEG SPLINTVinyl Technology, Inc.K874050INFLATABLE FOOT & ANKLE SPLINTVinyl Technology, Inc.K874053INFLATABLE FULL ARM SPLINTVinyl Technology, Inc.K853600INFLATABLE AIR SPLINTSHospitak, 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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