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Sanifix

by Iberhospitex, S.A.

510(k) K883983

Sanifix is a Class I device made by Iberhospitex, S.A., cleared under FDA 510(k) K883983 on 13 Dec 1988, active as of 22 Oct 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Source FDA 510(k), synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SN Traditional NumberK883983 Date13 Dec 1988DecidedStatusActive

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA product code
KGX
Device class
Class I
Regulation
21 CFR Part 880.5240
Advisory committee
General Hospital
FDA decision
SN

Similar devices

Other devices filed under FDA product code KGX (Tape And Bandage, Adhesive).

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