Prosurg, Inc.
Prosurg, Inc. holds FDA 510(k) medical device clearances, first cleared 2000, most recent 2016.
Top product codes for Prosurg, Inc.
Recent clearances by Prosurg, Inc.
- K152511 — Neo - Arthroscope (Rigid) 2.0mm/3.5mm, Outer sheath/ cannula, Outer sheath/ cannula w/ Handle, Trocar for outersheath/ cannula
- K152466 — Neo-Bronchoscope -Digital Video Bronchoscopy System(Rigid/Flexible)
- K152619 — Neoscope 3D - 3D Digital Video Endoscopic System (Rigid/Flexible)
- K120766 — ENDOSCOPIC DIAGNOSTIC & TREATMENT SYSTEM (MODIFICATION)
- K072528 — ADJUSTABLE BONE PLATES BIOABSORBABLE, SELF COMPRESSION BONE FIXATION SYSTEM & ACCESSORIES
- K071138 — CRANIOCLAMP BIOABSORBABLE CRANIAL BONE FLAP FIXATION SYSTEM
- K070737 — XSORB BIOABSORBABLE CRANIOFACIAL BONE FIXATION SYSTEM & ACCESSORIES
- K070846 — MINISLING ADJUSTABLE POLYMER SLING & SURGICAL MESH WITH SELF-ANCHORING SYSTEM
- K060326 — LASERTX - DIODE LASER & DELIVERY SYSTEM
- K050488 — TURBT-RF ELECTRODES AND ELECTROSURGICAL DEVICES
- K042780 — NEOSCOPE - ENDOSCOPIC DIAGNOSTIC & TREATMENT SYSTEM
- K030631 — ZIPPERE - BIOABSORBABLE/NON-ABSORBABLE POLYMER SLING & SURGICAL MESH
- K023257 — ENDOSCOPIC LASER DELIVERY SYSTEM-LASERTX
- K023051 — INTRAUTERINE DELIVERY SYSTEM - INJECTOR
- K001576 — EVA -VACUUM ASSIST DEVICE FOR CLITORAL THERAPY
- K000124 — SENSATION -VACUUM ASSIST DEVICES
Data sourced from openFDA. This site is unofficial and independent of the FDA.