PHOTOTHERAPY LAMP 900IW501JE PHOTOTHERAPY POWER MODULE 900IW502JE— 510(k) K002414
Substantially EquivalentFisher & Paykel Healthcare, Ltd.
FDA 510(k) clearance K002414 for PHOTOTHERAPY LAMP 900IW501JE PHOTOTHERAPY POWER MODULE 900IW502JE, Substantially Equivalent on 2000-09-25. Applicant: Fisher & Paykel Healthcare, Ltd.. Device class: 2.
Clearance details
- Applicant
- Fisher & Paykel Healthcare, Ltd.
- Product code
- Code LBI
- Device class
- Class 2
- Regulation
- 21 CFR 880.5700
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- East Tamaki, Auckland, NZ
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Data sourced from openFDA. This site is unofficial and independent of the FDA.