16 X 125 Mm Test Tube, Catalog #01-311

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

510(k) Number

K930372 ↗

FDA Product Code

KIR

Device Class

Class I

Regulation

21 CFR Part 864.2280

Advisory Committee

Hematology

FDA Decision

SESE Substantially Equivalent

• Cytoquant Mrc-5 Cells, Catalog #03-101

  Class I

  FDA 510(k) K924620 Active Cleared 7 Dec 1992

• Cytoquant Chlamydia Transport Medium

  Class I

  FDA 510(k) K961755 Active Cleared 17 May 1996

• Cytoquant Combined Transport Media

  Class I

  FDA 510(k) K924053 Active Cleared 15 Jan 1993

• One Dram Shell Vial, Catalog #02-261

  Class I

  FDA 510(k) K930393 Active Cleared 24 Mar 1993

• 16 X 25 Mm Test Tube, Catalog #01-461

  Class I

  FDA 510(k) K930366 Active Cleared 23 Mar 1993

• Cytoquant A-549 Cells, 16X125 Mm Tube #01-201

  Class I

  FDA 510(k) K924624 Active Cleared 7 Dec 1992

See all devices from Proteins Intl., Inc. →