DATASCOPE 6000 MONITOR— 510(k) K926099
Substantially EquivalentDatascope Corp.
FDA 510(k) clearance K926099 for DATASCOPE 6000 MONITOR, Substantially Equivalent on 1993-08-06. Applicant: Datascope Corp.. Device class: 2.
Clearance details
- Applicant
- Datascope Corp.
- Product code
- Code MLC
- Device class
- Class 2
- Regulation
- 21 CFR 870.2340
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Paramus, NJ, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.