Sterigage Integrator Test Pack for Steam Sterili.
FDA 510(k) K894399 · Pymah Corp.
510(k) numberK894399
Submission
- Device name
- Sterigage Integrator Test Pack for Steam Sterili.
- Applicant
- Pymah Corp.
Somerville, NJ, US - Received
- July 17, 1989
- Decision date
- September 11, 1989
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- FRC – Indicator, Biological Sterilization Process
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 880.2800
- Specialty
- General Hospital
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| K251452 | Celerity 5 HP Biological Indicator (LCB052); Celerity 5 HP Challenge Pack (LCB059)…FRC · Special | Steris | 06/06/2025SE |
| K250061 | Celerity IncubatorFRC · Special | STERIS Corporation | 02/06/2025SE |
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| K242453 | Terragene® Bionova® Photon Process Challenge Device with unique-point integrator…FRC · Traditional | Terragene S.A. | 12/12/2024SE |
| K242538 | 3M Attest Super Rapid Readout Biological Indicator 1493; 3M Attest Super Rapid Steam…FRC · Traditional | 3M Company | 11/25/2024SE |
| K241959 | 3M Attest Super Rapid Steam Clear Challenge Pack (1492PCD); 3M Attest Auto-reader…FRC · Traditional | 3M Company | 10/18/2024SE |
More from 3M Company
| 510(k) | Device | Decision |
|---|---|---|
| K952995 | Ati Ethylene Oxide Sterilization IndicatorJOJ · Traditional | 02/22/1996SE |
| K952408 | Ati Disposable Test Pack for Steam SterilizationJOJ · Traditional | 07/06/1995SE |
| K951063 | Ati Disposable Test Pack for Eo Gas SterilizationJOJ · Traditional | 05/10/1995SE |
| K934874 | Sterigage Eo 100%JOJ · Traditional | 04/18/1995SE |
| K943081 | Trimline 2000DXN · Traditional | 01/27/1995SE |
| K925745 | Ati(R) Disp Biological-Plus Test PackFRC · Traditional | 02/01/1994SE |
| K925496 | Ati Disposable Biological-Plus Test PackFRC · Traditional | 02/01/1994SE |
| K934180 | Slimline 3000DXQ · Traditional | 11/24/1993SE |
| K924681 | Glutaraldehyde MonitorsJOJ · Traditional | 11/17/1993SE |
| K925744 | Tempa-Kuff Single Pat Pre-Gaged Balanced Disp CuffDXQ · Traditional | 07/30/1993SE |
Questions and answers
When was Sterigage Integrator Test Pack for Steam Sterili. cleared by the FDA?
Sterigage Integrator Test Pack for Steam Sterili. (K894399) received a 510(k) decision of Substantially Equivalent on September 11, 1989, 56 days after the submission was received.
What is the product code of K894399?
The FDA product code is FRC – Indicator, Biological Sterilization Process, a Class II (moderate risk) device regulated under 21 CFR 880.2800.