THERMOMETER, MERCURY/CLINICAL— 510(k) K901790
Substantially EquivalentPerlink USA, Inc.
FDA 510(k) clearance K901790 for THERMOMETER, MERCURY/CLINICAL, Substantially Equivalent on 1990-07-11. Applicant: Perlink USA, Inc.. Device class: 2.
Clearance details
- Applicant
- Perlink USA, Inc.
- Product code
- Code FLK
- Device class
- Class 2
- Regulation
- 21 CFR 880.2920
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Rye, NY, US
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