Smiths Industries Medical Systems, Inc.
Smiths Industries Medical Systems, Inc. holds FDA 510(k) medical device clearances, first cleared 1993, most recent 1998.
Top product codes for Smiths Industries Medical Systems, Inc.
Recent clearances by Smiths Industries Medical Systems, Inc.
- K972385 — FENESTRATED FLEXIBLE D.I.C. TRACHEOSTOMY TUBE CUFFED
- K965017 — REGIONAL ANESTHESIA TRAYS
- K962175 — PORTEX ADJUSTABLE FLANGE TRACHEOSTOMY TUBE
- K962931 — SIMS PRO-VENT 250 (500) PLUS ARTERIAL BLOOD SAMPLING KIT
- K963570 — SIMS ADULT LUMBAR PUNCTURE KIT (4800-20,4801-20,4806-22,4807-22)
- K960429 — PER-FIT PERCUTANEOUS TRACHEOSTOMY KIT W/PORTEX TRACHEOSTMY TUBE & DISP. INNER CANNULA
- K953485 — SIMS CPAP SYSTEM
- K953483 — SIMS BLUE LINE ENDOBRONCHIAL TUBE
- K932946 — WALLACE IV CANNULA
- K932947 — WALLACE Y-CAN
- K952516 — PRO-VENT, LINE DRAW, PULSATOR
- K945777 — PRO-VENT(TM), PULSATOR(R), AND LINE DRAW(TM) ARTERIAL BLOOD SAMPLING SYRINGES
- K935927 — CONCORD/PORTEX EPIDURAL CATHETERS
- K942937 — SHARPSAFE CAT NO. 4105, 4115 AND 4120
- K936133 — PERCUTANEOUS TRACHEOSTOMY KIT
- K935776 — SHARPSAFE, CAT. NO. 4126
- K935777 — SHARPSAFE, CAT. NO. 4125
- K935603 — EXTRACORPOREAL TEMPERATURE SENSOR
- K935628 — SHARPSAFE CAT. NO. 4127
- K936134 — BERMAN AIRWAY
- K934465 — DIC TRACHEOSTOMY TUBE AND PORTEX BLUE LINE
- K931735 — BLUE LINE(R) PDT(TM) PORTEX DIRECTIONAL TUBE
Data sourced from openFDA. This site is unofficial and independent of the FDA.