KELLER VITAL SIGNS MONITOR - KMS-890
FDA 510(k) clearance K910262 · decided 1991-04-01
Clearance details
- K-number
- K910262
- Device name
- KELLER VITAL SIGNS MONITOR - KMS-890
- Applicant
- Keller Medical Specialties Products, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1991-01-22
- Decision date
- 1991-04-01
- Days to decision
- 69 days
- Clearance type
- Traditional
- Product code
- DSJ
- Device class
- 2
- Regulation number
- 870.1100
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Antioch, IL, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| EarlyVue VS30 (K190624) | Philips Medizin Systeme Boeblingen GmbH | 2019-10-27 |
| SureSigns VS3; SureSigns VS4 (K163649) | Philips Medical Systems | 2017-03-31 |
| SureSigns VS3, SureSigns VS4 (K151761) | Phillips Medical Systems | 2015-09-29 |
| SURESIGNS VS3, SURESIGNS VS4 (K133961) | Philips Medical Systems | 2014-06-26 |
| SAMS 8000 CARDIOPLEGIA MONITOR (K960916) | 3M Health Care, Sarns | 1996-06-04 |
Recalls involving this device
No recalls on record reference this clearance.