Hemoplus
FDA 510(k) K913622 · Sarstedt, Inc.
510(k) numberK913622
Submission
- Device name
- Hemoplus
- Applicant
- Sarstedt, Inc.
Newton, NC, US - Received
- August 14, 1991
- Decision date
- January 31, 1992
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- KHE – Reagent, Occult Blood
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 864.6550
- Specialty
- Hematology
Other 510(k)s with product code KHE
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K173212 | Instant-view-PLUS immunochemical Fecal Occult Blood TestKHE · Traditional | Alfa Scientific Designs, Inc. | 02/15/2018SE |
| K170548 | InSure ONEKHE · Traditional | Enterix, Inc. | 10/05/2017SE |
| K171484 | hema-screen SPECIFIC GoldKHE · Special | Immunostics Inc., | 06/14/2017SE |
| K162333 | Wondfo One Step Fecal Occult Blood (FOB) TestKHE · Traditional | Guangzhou Wondfo Biotech Co., Ltd. | 05/14/2017SE |
| K163554 | hema-screen ER XCEL Enhanced Readability Fecal Occult Blood TestKHE · Special | Immunostics Inc., | 01/17/2017SE |
| K143325 | OC-Light S FITKHE · Traditional | Eiken Chemical Co., Ltd. | 08/20/2015SE |
| K121397 | Osom Ifob 25 Test and Patient Collection Kit Osom Ifob Control Kit Osom Ifob 50 Test KitKHE · Traditional | SEKISUI Diagnostics, LLC | 12/28/2012SE |
| K113506 | Ind One Step Occult Blood (Fob) TestKHE · Special | Ind Diagnostics, Inc. | 12/19/2012SE |
| K110309 | Fob One Step Rapid TestKHE · Traditional | Orient Gene Biotech | 09/14/2011SE |
| K102664 | Hema Screen ErKHE · Special | Immunostics Inc., | 01/28/2011SE |
More from Immunostics Inc.,
| 510(k) | Device | Decision |
|---|---|---|
| K222801 | Safety LancetFMK · Traditional | 01/25/2023SE |
| K051019 | Safety NeedleJKA · Traditional | 07/25/2005SE |
| K032150 | Safety-MultiflyFPA · Traditional | 09/12/2003SE |
| K031359 | S-Monovette Edta K2-GELPJE · Traditional | 09/12/2003SE |
| K024237 | Urine Monovette Boric AcidJSM · Traditional | 04/14/2003SE |
| K003382 | Sarstedt Needle ProtectorFMI · Traditional | 03/30/2001SE |
Questions and answers
When was Hemoplus cleared by the FDA?
Hemoplus (K913622) received a 510(k) decision of Substantially Equivalent on January 31, 1992, 170 days after the submission was received.
What is the product code of K913622?
The FDA product code is KHE – Reagent, Occult Blood, a Class II (moderate risk) device regulated under 21 CFR 864.6550.