Skip to content

Pajunk Infiltralong Wound Infiltration Catheter Kit

by Pajunk GmbH Medizintechnologie 510(k)

Active United States

510(k) K080675

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK080675 Date20 Jun 2008ClearedStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

510(k)

510(k) Number
FDA Product Code
BSO
Device Class
Class II
Regulation
21 CFR Part 868.5120
Advisory Committee
Anesthesiology
FDA Decision
SESE Substantially Equivalent

Other devices from Pajunk GmbH Medizintechnologie

See all devices from Pajunk GmbH Medizintechnologie →