PHILIPS TELESCAN— 510(k) K911773
Substantially EquivalentPhilips Medical Systems, Inc.
FDA 510(k) clearance K911773 for PHILIPS TELESCAN, Substantially Equivalent on 1991-06-28. Applicant: Philips Medical Systems, Inc.. Device class: 1.
Clearance details
- Applicant
- Philips Medical Systems, Inc.
- Product code
- Code LMD
- Device class
- Class 1
- Regulation
- 21 CFR 892.2020
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- 5680 Da Best, NL
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Data sourced from openFDA. This site is unofficial and independent of the FDA.