STERILIZATION INDICATOR FOR FLASH STERILIZATION— 510(k) K871672

Name: FDA 510(k) clearance K871672
Creator: U.S. Food and Drug Administration
Published: 1987-06-01

Substantially Equivalent

Propper Mfg. Co., Inc.

FDA 510(k) clearance K871672 for STERILIZATION INDICATOR FOR FLASH STERILIZATION, Substantially Equivalent on 1987-06-01. Applicant: Propper Mfg. Co., Inc.. Device class: 2.

Clearance details

Applicant: Propper Mfg. Co., Inc.
Product code: Code LRT
Device class: Class 2
Regulation: 21 CFR 880.2800
Advisory panel: General Hospital
Date received: 1987-04-28
Decision date: 1987-06-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Long Island City, NY, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LRT

view all

K002937 — TST CONTROL INTEGRATOR FOR STEAM STERILIZERS2001-11-05
K965154 — TST CONTROL INTEGRATOR FOR STEAM AUTOCLAVE1997-09-19
K951113 — CROSS-CHECKS1996-08-19
K951703 — TAMPER EVIDENT ARROWS WITH AND WITHOUT STERILIZATION INDICATORS1995-06-28

More clearances from Propper Mfg. Co., Inc.

view all

K111453 — STEAM DOT BLU PROCESS INDICATOR2012-04-05
K102894 — CLASSIX CHEMICAL STERILIZATION INDICATOR2011-05-25
K082620 — ONCE-A-DAY VERTOS TEST PACK2009-07-08
K031152 — PROPPER VAPOR LINE PCD (STEAM STERILIZATION PROCESS CHALLENGE TEST)2004-08-17
K991618 — BI-O.K. SELF-CONTAINED BIOLOGICAL INDICATOR2001-01-24

Data sourced from openFDA. This site is unofficial and independent of the FDA.