Valtrac (Bar) Remover Device

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K863752 ↗

FDA Product Code

EMF

Device Class

Class I

Regulation

21 CFR Part 878.4800

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

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• Argyle Quick- Picc Peripherally Inserted Central Catheter- Picc Trays, Argyle Quick- Picc Peripherally Inserted Central

  Class II

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  FDA 510(k) K953425 Active Cleared 21 Aug 1995

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  FDA 510(k) K811191 Active Cleared 27 May 1981

• Biofix* Biodegradable Fixation Rod

  Class II

  FDA 510(k) K890902 Active Cleared 3 Nov 1989

See all devices from Davis & Geck, Inc. →