# Propper Mfg. Co., Inc.

- Location (FDA's records): Long Island, NY
- FDA decisions: 25 (1977–2012): 25 510(k) clearances
- Product codes: JOJ (11), FRC (4), GCP (3), KHE (3), CCW (1), LRT (1), OCX (1), FRG (1)
- Predicates its devices cite: 4 (2 its own); citations of its devices by later devices: 4 (2 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- STERIS Corporation: 2 (https://510kreport.com/company/steris)

## Firms that cite its devices most
- Girgis Scope, LLC: 1 (https://510kreport.com/company/girgis-scope)
- Spsmedical Supply Corp.: 1 (https://510kreport.com/company/spsmedical-supply)

## Its most-cited devices
- K915804: Propper Laryngoscope Blades W Fiber Optic Illum. (1992), cited by 1
- K991276: Pass/Fail Challenge Pack (1999), cited by 1
- K895910: Steamline (1990), cited by 1
- K961156: Once-a-Day  Bowie and Dick Test Pack. (1997), cited by 1

## Recent decisions
- K111453: Steam Dot Blu Process Indicator (Apr 5, 2012)
- K102894: Classix Chemical Sterilization Indicator (May 25, 2011)
- K082620: Once-a-Day Vertos Test Pack (Jul 8, 2009)
- K031152: Propper Vapor Line PCD (Steam Sterilization Process Challenge Test) (Aug 17, 2004)
- K991618: BI-O.K. Self-Contained Biological Indicator (Jan 24, 2001)
- K991276: Pass/Fail Challenge Pack (Jul 12, 1999)
- K973585: Propper EO Line Ethylene Oxide Sterilization Integrator (Nov 6, 1998)
- K972747: BI-O.K. EO Gas Biological Test-Pak (269305,269310,269320) (Jan 9, 1998)

Source page: https://510kreport.com/company/propper-mfg