Medical Device Manufacturer · US , Great Neck , NY

Mist, Inc. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1995

8

Total

8

Cleared

0

Denied

Mist, Inc. has 8 FDA 510(k) cleared medical devices. Based in Great Neck, US.

Historical record: 8 cleared submissions from 1995 to 1997. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Mist, Inc. Filter by specialty or product code using the sidebar.

Mist, 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 - Mist, Inc.

8 devices

1-8 of 8

Cleared Sep 26, 1997

MIST MICRO INTERCHANGEABLE SCOPE SYSTEM (TM)

General & Plastic Surgery · 197d

Cleared Sep 23, 1997

MIST PANORAMIC LAPAROSCOPE A RIGID LAPAROSCOPE

General & Plastic Surgery · 179d

Cleared Jun 23, 1995

MIST ELECTROSURGICAL PROBES, VARIOUS STYLES & SIZES, SURGICAL INSTRUMENTS...

General & Plastic Surgery · 38d

Cleared Jun 23, 1995

MIST ELECTROSURGICAL PROBES, VARIOUS STYLES & SIZES

General & Plastic Surgery · 36d

Cleared May 12, 1995

MIST ENDOSCOPIC NEEDLES

Gastroenterology & Urology · 32d

Cleared May 03, 1995

General & Plastic Surgery · 34d

Cleared May 03, 1995

MIST ENDOSCOPIC CANNULAS

General & Plastic Surgery · 34d

Cleared May 03, 1995

MIST ENDOSCOPIC PROBES

General & Plastic Surgery · 21d