Miniscope MS-3
FDA 510(k) K954066 · Schiller America, Inc.
510(k) numberK954066
Submission
- Device name
- Miniscope MS-3
- Applicant
- Schiller America, Inc.
Tustin, CA, US - Received
- August 30, 1995
- Decision date
- October 27, 1995
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Device classification
- Product code
- DPS – Electrocardiograph
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.2340
- Specialty
- Cardiovascular
Other 510(k)s with product code DPS
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K252463 | SE-1202 Series Electrocardiograph (Model: SE-1202, SE-1202E)DPS · Traditional | Edan Instruments, Inc. | 07/02/2026SE |
| K251670 | MAC 7 Resting ECG Analysis SystemDPS · Traditional | Ge Medical Systems Information Technologies, Inc. | 01/26/2026SE |
| K252361 | AccurECG Analysis System (v2.0)DPS · Traditional | Accurkardia, Inc. | 12/22/2025SE |
| K252474 | Withings BeamO (SCT02)DPS · Traditional | Withings | 11/10/2025SE |
| K250569 | Cardiologs Holter PlatformDPS · Traditional | Philips France Commercial | 08/06/2025SE |
| K243252 | ZBPro DiagnosticDPS · Traditional | Zbeats, Inc. | 07/10/2025SE |
| K243305 | Masimo W1DPS · Traditional | Masimo Corporation | 04/03/2025SE |
| K241217 | CloudHRV System (100-01-001)DPS · Traditional | Inmedix, Inc. | 01/16/2025SE |
| K241556 | Cardiac Workstation (5000); Cardiac Workstation (7000)DPS · Traditional | Philips Medizin Systeme Böblingen GmbH | 12/17/2024SE |
| K240229 | Masimo W1DPS · Traditional | Masimo Corporation | 08/08/2024SE |
More from Masimo Corporation
| 510(k) | Device | Decision |
|---|---|---|
| K973751 | MT-200DQK · Traditional | 08/25/1998SE |
| K973735 | Microvit MT-100DSH · Traditional | 08/25/1998SE |
| K970879 | Cardiovit CS-200LOS · Traditional | 06/25/1997SE |
| K953396 | Cardiovit AT-1C, AT-2CLOS · Traditional | 12/19/1995SE |
| K941462 | Cardiovit AT-5CLOS · Traditional | 05/19/1995SE |
| K946205 | Cardiovit AT-1, P-80DPS · Traditional | 03/16/1995SE |
| K914970 | Cardiovit CS-100LOS · Traditional | 11/03/1992SE |
| K896121 | Schiller Model SP-200 Spirovit(Tm)BZG · Traditional | 01/09/1990SE |
| K896120 | Schiller Model SP-100 Spirovit(Tm)BZG · Traditional | 01/09/1990SE |
Questions and answers
When was Miniscope MS-3 cleared by the FDA?
Miniscope MS-3 (K954066) received a 510(k) decision of Substantially Equivalent on October 27, 1995, 58 days after the submission was received.
What is the product code of K954066?
The FDA product code is DPS – Electrocardiograph, a Class II (moderate risk) device regulated under 21 CFR 870.2340.