Medical Device Manufacturer · US , Mchenry , IL

Smith & Nephew, Mpl Division - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1976

Total

Cleared

Denied

Smith & Nephew, Mpl Division has 9 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 9 cleared submissions from 1976 to 1984. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Smith & Nephew, Mpl Division Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Smith & Nephew, Mpl Division

9 devices

1-9 of 9

Cleared Sep 27, 1984

MPL HYPO BRAND BREECH LOAD ASPIR SYRINGE

K843314 · EJI

Dental · 34d

Cleared May 21, 1984

SOLOPAK BRAND FILTER NEEDLE W/5 MICRO

K841280 · FPB

General Hospital · 54d

Cleared Apr 05, 1984

MAX-I-PROBE PERIODONTAL ENDODONTIC PROB

K840237 · EIC

Dental · 76d

Cleared Mar 30, 1984

HYPO BRAND DISPOS. DENTAL NEEDLES-PLAST

K833304 · DZM

Dental · 189d

Cleared Aug 12, 1983

MICRO Z DISPOS. SPINAL ANESTH. NEEDLE

K832126 · BSP

Anesthesiology · 42d

Cleared Jul 12, 1983

HERAPIN LOCK FLUSH SOLUTION USE KIT

K831765 · FMI

Hematology · 41d

Cleared Mar 24, 1983

HENKE JECT PRESSURE SYRINGE

K830524 · EJI

Dental · 35d

Cleared Feb 15, 1983

MICRO 2 HYPODERMIC NEEDLES

K830242 · FMI

General Hospital · 21d

Smith & Nephew, Mpl Division - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Smith & Nephew, Mpl Division

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