Medical Device Manufacturer · US , Hollywood , FL

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

13 submissions · 13 cleared · Since 1987

Total

Cleared

Denied

Solway, Inc. has 13 FDA 510(k) cleared medical devices. Based in Hollywood, US.

Historical record: 13 cleared submissions from 1987 to 1988.

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

FDA 510(k) Regulatory Record - Solway, Inc.

13 devices

1-13 of 13

Cleared Feb 05, 1988

CARDIOVASCULAR SURGICAL INSTRUMENTS

K874960 · DWS

Cardiovascular · 65d

Cleared Feb 02, 1988

FORCEPS CLIPRACK VENTRICULAR CANNULA SAWS SPATULAS

K874962 · HAO

Neurology · 62d

Cleared Jan 28, 1988

SELF-RETAINING RETRACTOR FOR NEUROSURGERY

K874956 · GZT

Neurology · 57d

Cleared Jan 27, 1988

DENTAL HAND INSTRUMENTS

K874964 · EKJ

Dental · 56d

Cleared Jan 22, 1988

RONGEUR (NEUROSURGICAL INSTRUMENTS)

MICROSURGICAL INSTRUMENTS

K874950 · HTD

General & Plastic Surgery · 28d

Cleared Dec 30, 1987

MANUAL CRANIAL DRILL, BURR, TREPHINE & ACCESSORIES

General & Plastic Surgery · 28d

Cleared Dec 30, 1987

BONE CUTTING INSTRUMENTS & ACCESSORIES

K874961 · GDR

General & Plastic Surgery · 28d

Cleared Dec 30, 1987

MANUAL SURGICAL INSTRUMENTS FOR GENERAL USE

K874965 · HTD

General & Plastic Surgery · 28d

Cleared Dec 23, 1987

MANUAL OPHTHALMIC SURGICAL INSTRUMENTS

K874963 · HNA

Ophthalmic · 21d

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

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