Manifold Contrast Vision Meter

FDA registration

ADAPTIVE SENSORY TECHNOLOGY INC·1 product·🇺🇸 United States

NPA de México S. de R.L. de C.V.

FDA registration

NPA de México S. de R.L. de C.V.·1 product·🇲🇽 Mexico

Frax Pro

FDA registration

NPA de México S. de R.L. de C.V.·1 product·🇲🇽 Mexico

Welch Allyn, Inc.

FDA UDI

WELCH ALLYN, INC.·00732094225433·CUFF TL REUSE ADULT DBL BARREL

Welch Allyn, Inc.

FDA UDI

WELCH ALLYN, INC.·00732094225457·CUFF TL REUSE CHILD DBL BARREL

Welch Allyn, Inc.

FDA UDI

WELCH ALLYN, INC.·00732094225440·CUFF TL REUSE SMALL ADULT DBL BARREL

Welch Allyn, Inc.

FDA UDI

WELCH ALLYN, INC.·00732094225426·CUFF TL REUSE ADULT LONG DBL BARREL

Welch Allyn, Inc.

FDA UDI

WELCH ALLYN, INC.·00732094225464·CUFF TL REUSE INFANT DBL BARREL

Welch Allyn, Inc.

FDA UDI

WELCH ALLYN, INC.·00732094225419·CUFF TL REUSE LARGE ADULT DBL BARREL

Welch Allyn, Inc.

FDA UDI

WELCH ALLYN, INC.·00732094225396·CUFF TL REUSE THIGH DBL BARREL

Welch Allyn, Inc.

FDA UDI

WELCH ALLYN, INC.·00732094225402·CUFF TL REUSE LARGE ADULT LONG DBL B

Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)

FDA Pre-Market Approval

FDA Class 3 ·CONTAK CD (MODEL 1823), CONTAK CD 2 (MODELS H115 AND H119), RENEWAL (MODEL H135), RENEWAL 3 (MODELS H170, H175, H177, A

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·CONTAK CD2, CONTAK RENEWAL/RENEWAL 3/ RENEWAL 3/3HE RF

STATION,MUSH.BTN,C.B. LCK,1-NO,1-NC

FDA UDI

Crest Healthcare Supply·B48415343120B0·STATION, MUSHROOM BUTTON, CODE BLUE, LOCKING

PUREtrace™

FDA 510(k)

FDA Class 2 ·Obstetrics/Gynecology

Zimed Distal Medial Tibial Plate and Screw System

FDA 510(k)

FDA Class 2 ·Orthopedic

BLUE LINE ULTRA SUCTIONAID TRACHEOSTOMY TUBE

FDA 510(k)

FDA Class 2 ·Anesthesiology

Small Volume 0.2mL Syringe

FDA 510(k)

FDA Class 2 ·General Hospital

VITALSAT PULSE OXIMETER, MODEL IC32000

FDA 510(k)

FDA Class 2 ·Cardiovascular

WALLACE (SURE VIEW) EMBRYO REPLACEMENT CATHETER AND TRIAL TRANSFER CATHETER

FDA 510(k)

FDA Class 2 ·Obstetrics/Gynecology