FDA 510(k)

SOFT SOCK

K-Number: K944240 · 1994-12-27

Decision Date1994-12-27

Product CodeFQL

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

SOFT SOCK is the device name listed in this FDA 510(k) record. The listed applicant is Silipos, Inc.. It received FDA 510(k) clearance on 1994-12-27 under 510(k) number K944240. The device is classified under product code FQL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOFT SOCK?

SOFT SOCK is a medical device that received FDA 510(k) clearance on 1994-12-27. The listed applicant is Silipos, Inc.. The 510(k) number is K944240.

When did SOFT SOCK receive FDA 510(k) clearance?

SOFT SOCK received FDA 510(k) clearance on 1994-12-27, under 510(k) number K944240.

Who is the listed applicant for SOFT SOCK?

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

What is the FDA product code for SOFT SOCK?

The FDA product code for SOFT SOCK is FQL.

Other records listing Silipos, 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.

K955664STERILIZED TRI BLOCK POLYMER GEL SHEET K942695TRI BLOCK POLUMER GEL SHEETING K932048SILICONE GEL SHEETING

Related Devices (Code: FQL)

K823789ELASTIC COMPRESSION ANKLETOrthopaedic Resources Corp.K823350ELASTIC COMPRESSION ANKLETPodiatry Products Corp.K821260VITOFITSelomas, Inc.K821259VITASANSelomas, Inc.K820484VENES CUSTON RXJung Products, 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.