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Pathromtin Sl

by Behring Diagnostics, Inc. 510(k)

Active United States

510(k) K955450

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK955450 Date19 Apr 1996ClearedStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Recalls

1 recall · FDA

    • Terminated Z-0773-04 FDA Unclassified (pre-2012) initiated 1 Mar 2004

    cloudy appearance or precipitate

Specification

510(k)

510(k) Number
FDA Product Code
GFO
Device Class
Class II
Regulation
21 CFR Part 864.7925
Advisory Committee
Hematology
FDA Decision
SESE Substantially Equivalent

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