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FDA 510(k)

INFLATABLE FOOT & ANKLE SPLINT

K-Number: K874050 · 1987-11-23

ApplicantVinyl Technology, Inc.
Decision Date1987-11-23
Product CodeFZF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

INFLATABLE FOOT & ANKLE SPLINT is the device name listed in this FDA 510(k) record. The listed applicant is Vinyl Technology, Inc.. It received FDA 510(k) clearance on 1987-11-23 under 510(k) number K874050. 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 INFLATABLE FOOT & ANKLE SPLINT?

INFLATABLE FOOT & ANKLE SPLINT is a medical device that received FDA 510(k) clearance on 1987-11-23. The listed applicant is Vinyl Technology, Inc.. The 510(k) number is K874050.

When did INFLATABLE FOOT & ANKLE SPLINT receive FDA 510(k) clearance?

INFLATABLE FOOT & ANKLE SPLINT received FDA 510(k) clearance on 1987-11-23, under 510(k) number K874050.

Who is the listed applicant for INFLATABLE FOOT & ANKLE SPLINT?

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

What is the FDA product code for INFLATABLE FOOT & ANKLE SPLINT?

The FDA product code for INFLATABLE FOOT & ANKLE SPLINT is FZF.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Vinyl Technology, 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.

K874774TROUSERS, PNEUMATIC, ANTI-SHOCK THREE BLADDERSK874051INFLATABLE FULL LEG SPLINTK874052INFLATABLE HALF LEG SPLINTK874053INFLATABLE FULL ARM SPLINT

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.K874053INFLATABLE FULL ARM SPLINTVinyl Technology, Inc.K853600INFLATABLE AIR SPLINTSHospitak, Inc.K831764URIAS PRESSURE SPLINTS, & FIRST AIDSvenol Andersen

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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