PERIFLUX PF4001 LASER DOPPLER FLOWMETER— 510(k) K922368
Substantially EquivalentPerimed, Inc.
FDA 510(k) clearance K922368 for PERIFLUX PF4001 LASER DOPPLER FLOWMETER, Substantially Equivalent on 1993-02-03. Applicant: Perimed, Inc.. Device class: 2.
Clearance details
- Applicant
- Perimed, Inc.
- Product code
- Code DPW
- Device class
- Class 2
- Regulation
- 21 CFR 870.2100
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Piscataway, NJ, US
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