Chlamydia Group Cf Antigen

No FDA recalls found in the data synced 11 Oct 2026.

510(k) Number

K844868 ↗

FDA Product Code

GPW

Device Class

Class I

Regulation

21 CFR Part 866.3120

Advisory Committee

Microbiology

FDA Decision

SESE Substantially Equivalent

• Herpes-Iha Kit

  Class I

  FDA 510(k) K822095 Active Cleared 5 Apr 1983

• Cmv Cf Antigen

  Class II

  FDA 510(k) K853277 Active Cleared 7 Nov 1985

• Mycoplasma Pneumoniae Cf Antigen

  Class I

  FDA 510(k) K834338 Active Cleared 27 Feb 1984

• Arbovirus Igm Ifa Test

  Class I

  FDA 510(k) K913618 Active Cleared 3 Dec 1992

• Herpes Simplex Group Cf Antigen

  Class II

  FDA 510(k) K850609 Active Cleared 9 May 1985

• Polio Type I Cf Antigen, & Type II, III

  Class I

  FDA 510(k) K853278 Active Cleared 7 Nov 1985

See all devices from Hillcrest Biologicals →