Medical Device Manufacturer · US , Devers , MA

Microline Pentax, Inc. - FDA 510(k) Cleared Devices

12 submissions · 12 cleared · Since 1988

Total

Cleared

Denied

Microline Pentax, Inc. has 12 FDA 510(k) cleared general & plastic surgery devices. Based in Devers, US.

Historical record: 12 cleared submissions from 1988 to 2002.

Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.

Microline Pentax, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Microline Pentax, Inc.

12 devices

1-12 of 12

Cleared Jan 08, 2002

MICROLINE INC. REUSABLE LAPAROSCOPIC CLIP APPLIER WITH IMPLANTABLE TITANIUM...

K013695 · GCJ

General & Plastic Surgery · 62d

Cleared Oct 21, 1998

ACCUSHEAR LAPAROSCOPIC SURGICAL INSTRUMENTS

K982984 · GEI

General & Plastic Surgery · 56d

Cleared May 29, 1998

DISPOSABLE RE-NEW FORCEPS

K981389 · GEI

General & Plastic Surgery · 43d

Cleared May 20, 1998

ELECTROSURGICAL CAUTERY PROBES

K981188 · GEI

General & Plastic Surgery · 48d

Cleared Mar 27, 1998

3 MM SELEC-TIP LAPAROSCOPIC SCISSORS

K980758 · GEI

General & Plastic Surgery · 28d

Cleared Jan 22, 1998

RE-NEW FORCEPS LAPAROSCOPIC SURGICAL TIPS

K974066 · GEI

General & Plastic Surgery · 87d

Cleared Mar 28, 1997

SELECTA-TIP LAPAROSCOPIC SCISSORS

K970826 · GEI

General & Plastic Surgery · 22d

Cleared Aug 09, 1996

RE-NEW LAPAROSCOPIC INSTRUMENTS

K962119 · GEI

General & Plastic Surgery · 70d

Cleared Oct 12, 1993

QUICK SWITCH LAPAROSCOPIC INSTRUMENTS

K932648 · GCJ

General & Plastic Surgery · 132d

Cleared Apr 04, 1990

INTRAOCULAR MICROSCISSORS BY MEANS OF GAMMA RADIA.

K897093 · HNF

Ophthalmic · 105d

Cleared Sep 12, 1988

BRADBURY INTRAOCULAR RETINAL KIT CAT #200

Microline Pentax, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Microline Pentax, Inc.

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