Prochek G Glutaraldehyde Concentration Level Indicator
FDA 510(k) K960089 · Cottrell, Ltd.
510(k) numberK960089
Submission
- Device name
- Prochek G Glutaraldehyde Concentration Level Indicator
- Applicant
- Cottrell, Ltd.
North Attleboro, MA, US - Received
- January 11, 1996
- Decision date
- April 4, 1996
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- JOJ – Indicator, Physical/Chemical Sterilization Process
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 880.2800
- Specialty
- General Hospital
Other 510(k)s with product code JOJ
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K260181 | LF Process Indicator Tape for Steam SterilizationJOJ · Special | Intertape Polymer Group | 02/20/2026SE |
| K251991 | SafeSecure Steam Sterilization Process Indicator (4012, 4013, 4014, 4016); SafeSecure…JOJ · Traditional | Shenzhen Safesecure Medical Infection Control… | 12/23/2025SE |
| K251035 | DISINTEK PA Test StripsJOJ · Traditional | Serim Research | 06/03/2025SE |
| K251048 | Rapicide PA High-Level Disinfection Test Strip Model Ref # = ML02-0118JOJ · Special | STERIS Corporation | 05/02/2025SE |
| K243876 | VERIFY STEAM Integrating IndicatorJOJ · Special | STERIS Corporation | 04/25/2025SE |
| K250172 | Green Card Bowie-Dick Test (BD115)JOJ · Special | Steritec Products, Inc. (A Getinge Company) | 02/20/2025SE |
| K242860 | Type 5 Integrating Indicator for Steam (CSPN-15)JOJ · Traditional | True Indicating, LLC | 01/17/2025SE |
| K241036 | Autoclave Indicator Tape; EO Indicator TapeJOJ · Traditional | Jiangmen New Era External Use Drug Co., Ltd. | 12/17/2024SE |
| K243475 | Chemical Indicator for enspire CLCSPS (LCC015)JOJ · Special | STERIS Corporation | 12/04/2024SE |
| K242795 | Getinge Assured MI Steam Migrating IntegratorJOJ · Special | Steritec Products Mfg. (A Getinge Group Company) | 10/15/2024SE |
More from Steritec Products Mfg. (A Getinge Group Company)
| 510(k) | Device | Decision |
|---|---|---|
| K972708 | Endo-Spor Plus / HyprocideMED · Traditional | 09/13/1999SE |
| K970726 | VapocideMED · Traditional | 05/18/1998SE |
| K952241 | Protouch OvergloveMMP · Traditional | 08/07/1995SE |
| K952234 | Barrier All FilmEFS · Traditional | 07/31/1995SE |
| K932922 | Procide 14 N.S., Omnicide/Liquid & Plus Liq ActivatorMED · Traditional | 07/03/1995SE |
| K951983 | Imni-IiLRJ · Traditional | 06/20/1995SE |
| K945575 | Pro Barrier(Tm) Tube Sox(Tm)MMN · Traditional | 03/06/1995SE |
| K893802 | Proview Self-Sealing Sterilization PouchKCT · Traditional | 04/04/1990SE |
Questions and answers
When was Prochek G Glutaraldehyde Concentration Level Indicator cleared by the FDA?
Prochek G Glutaraldehyde Concentration Level Indicator (K960089) received a 510(k) decision of Substantially Equivalent on April 4, 1996, 84 days after the submission was received.
What is the product code of K960089?
The FDA product code is JOJ – Indicator, Physical/Chemical Sterilization Process, a Class II (moderate risk) device regulated under 21 CFR 880.2800.