HEADLAMP HL2000.— 510(k) K994362
Substantially EquivalentAngiolaz, Inc.
FDA 510(k) clearance K994362 for HEADLAMP HL2000., Substantially Equivalent on 2000-05-11. Applicant: Angiolaz, Inc.. Device class: 2.
Clearance details
- Applicant
- Angiolaz, Inc.
- Product code
- Code FSR
- Device class
- Class 2
- Regulation
- 21 CFR 886.4335
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Bellows Falls, VT, US
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