Medical Device Manufacturer · US , Chesterfield , MO

Surgical Technologies, Inc. - FDA 510(k) Cleared Devices

28 submissions · 28 cleared · Since 1991

Total

Cleared

Denied

Surgical Technologies, Inc. has 28 FDA 510(k) cleared medical devices. Based in Chesterfield, US.

Historical record: 28 cleared submissions from 1991 to 1995.

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

FDA 510(k) Regulatory Record - Surgical Technologies, Inc.

28 devices

1-12 of 28

Cleared Nov 30, 1995

CYSTOSCOPE

K941992 · FBO

Gastroenterology & Urology · 584d

INFINITECH LIGHTED INFUSION CANNULA

SURGICAL TECHNOLOGIES, INC. SYRINGE

K951918 · FMF

General Hospital · 87d

INFINITECH ASPIRATING LASER PROBE

K946135 · HQE

Ophthalmic · 123d

Cleared Mar 14, 1995

INFINITECH SOFT TIP FLUTE NEEDLE

Gastroenterology & Urology · 62d

Cleared Jun 14, 1994

PRESSURE MONITORING EXTENSION

K942482 · DQO

Cardiovascular · 20d

Cleared May 04, 1994

FLEXIBLE GRASPING FORCEPS

K941161 · EOQ

Ear, Nose, Throat · 54d

Cleared Apr 28, 1994

FLEXIBLE BIOPSY CUP FORCEPS

K941158 · EOQ

Ear, Nose, Throat · 48d

Surgical Technologies, Inc. - FDA 510(k) Cleared Devices

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