Sakura DRS-60 Automatic Slide Stainer
FDA 510(k) K874897 · Sakura Finetek U.S.A., Inc.
510(k) numberK874897
Submission
- Device name
- Sakura DRS-60 Automatic Slide Stainer
- Applicant
- Sakura Finetek U.S.A., Inc.
Torrance, CA, US - Received
- December 1, 1987
- Decision date
- January 5, 1988
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Other 510(k)s with product code KPA
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K933996 | ProfiblotKPA · Traditional | Tecan U.S., Ltd. | 01/28/1994SE |
| K884258 | VersablotKPA · Traditional | American Bionetics, Inc. | 12/14/1988SE |
| K881592 | Wescor Model 7300 Aerospray Gram StainerKPA · Traditional | Wescor, Inc. | 05/13/1988SE |
| K880745 | LX-100 Slide StainerKPA · Traditional | Innovative Medical Systems, Inc. | 04/27/1988SE |
| K874887 | Wesblot ProcessorKPA · Traditional | American Bionetics, Inc. | 03/24/1988SE |
| K872916 | Histomatic Slide Stainer, Code-On VersionKPA · Traditional | Fisher Scientific Co., LLC | 09/14/1987SE |
| K853210 | MST-1050-II X-Ray UnitKPA · Traditional | Radiological Engineering, Inc. | 10/10/1985SE |
| K850333 | Pump Tube Sets for Hema-Tek I & II Slide StainersKPA · Traditional | Shaban Mfg. Co. | 02/27/1985SE |
| K850157 | Cannulas for Hema-Tek I & KK Slide StainersKPA · Traditional | Shaban Mfg. Co. | 02/27/1985SE |
| K842077 | Midas II Automatic StainerKPA · Traditional | Innovative Medical Systems, Inc. | 07/27/1984SE |
More from Innovative Medical Systems, Inc.
Questions and answers
When was Sakura DRS-60 Automatic Slide Stainer cleared by the FDA?
Sakura DRS-60 Automatic Slide Stainer (K874897) received a 510(k) decision of Substantially Equivalent on January 5, 1988, 35 days after the submission was received.
What is the product code of K874897?
The FDA product code is KPA – Slide Stainer, Automated, a Class I (low risk) device regulated under 21 CFR 864.3800.