Laser Peripherals, LLC
Laser Peripherals, LLC holds FDA 510(k) medical device clearances, first cleared 1988, most recent 2017, with 1 FDA device recall on record.
Top product codes for Laser Peripherals, LLC
FDA recalls by Laser Peripherals, LLC
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Laser Peripherals, LLC
- K170366 — Laser Peripherals, LLC Family of Bare Laser Fibers
- K030959 — BARE LASER FIBER MODELS DBLF-40, DBLF-60, DBLF-60-1, DCLF-600B, DSLF-60, DBLF-100
- K011207 — LASER PERIPHERALS REUSABLE HOLMIUM FIBER
- K992083 — SCATTERFREE LATERAL EMITTING FIBER
- K974229 — LS-905 FIBERCHOICE ADAPTER SYSTEM
- K972272 — LASER PERIPHERALS HOLMIUM BARE FIBERS
- K961516 — LASER PERIPHERALS INC. BARE FIBER
- K961079 — LASER PERIPHERALS INC. SCATTERFREE FIBER
- K901786 — LASEGUIDE CAT # CLF-600D & CLF-1000D
- K880591 — LASEGUIDE 600A, 600B, 400A, 400B FOR OB-GYN USE
- K880592 — LASEGUIDE 600A, 600B, 400A, 400B FOR PULMONARY USE
- K874680 — LASEGUIDE 600A, 600B, 400A, AND 400B
Data sourced from openFDA. This site is unofficial and independent of the FDA.