Microline Pentax, Inc.
Microline Pentax, Inc. holds FDA 510(k) medical device clearances, first cleared 1988, most recent 2002.
Top product codes for Microline Pentax, Inc.
Recent clearances by Microline Pentax, Inc.
- K013695 — MICROLINE INC. REUSABLE LAPAROSCOPIC CLIP APPLIER WITH IMPLANTABLE TITANIUM CLIPS, MODEL M/L-10
- K982984 — ACCUSHEAR LAPAROSCOPIC SURGICAL INSTRUMENTS
- K981389 — DISPOSABLE RE-NEW FORCEPS
- K981188 — ELECTROSURGICAL CAUTERY PROBES
- K980758 — 3 MM SELEC-TIP LAPAROSCOPIC SCISSORS
- K974066 — RE-NEW FORCEPS LAPAROSCOPIC SURGICAL TIPS
- K970826 — SELECTA-TIP LAPAROSCOPIC SCISSORS
- K962119 — RE-NEW LAPAROSCOPIC INSTRUMENTS
- K932648 — QUICK SWITCH LAPAROSCOPIC INSTRUMENTS
- K897093 — INTRAOCULAR MICROSCISSORS BY MEANS OF GAMMA RADIA.
- K881049 — BRADBURY INTRAOCULAR RETINAL KIT CAT #200
- K880943 — MICROLINE CAT #100
Data sourced from openFDA. This site is unofficial and independent of the FDA.