Prochem

FDA UDI

VIVAPRODUCTS, INC.·00860002864877·BJP PROTEIN CONCENTRATOR 20ml, 100 TESTS

KCP PAK #2 CONVENIENCE PACK MODIFICATION

FDA 510(k)

FDA Class 2 ·Ophthalmic

ADAPTOR: KAPS CINE TO MOELLER BEAMSPLITTER

FDA 510(k)

FDA Class 1 ·General, Plastic Surgery

KCP (KELMAN COMPACT PHACO-EMULSIFIER) PEA

FDA 510(k)

FDA Class 2 ·Ophthalmic

Calibration Gas Mixture, Lung Diffusion Test Mixture, Clinical Blood Gas Mixture

FDA registration

NEXAIR, LLC·1 product·🇺🇸 United States

Aquilo Sports CT1000

FDA registration

AQUILO SPORTS L.L.C.·1 product·🇺🇸 United States

Laser Gas Mixture

FDA registration

NEXAIR, LLC·1 product·🇺🇸 United States

Laser Gas Mixture

FDA registration

NEXAIR, LLC.·1 product·🇺🇸 United States

Calibration Gas Mixture, Lung Diffusion Test Mixture, Clinical Blood Gas Mixture

FDA registration

NEXAIR, LLC.·1 product·🇺🇸 United States

Aquilo Sports CCT1500 System

FDA registration

AQUILO SPORTS L.L.C.·1 product·🇺🇸 United States

Anti-Kpa

FDA UDI

AMERICAN NATIONAL RED CROSS·00858400005022·Blood Grouping Reagent

Anti-Kpa

FDA UDI

IMMUCOR, INC.·10888234000778·This reagent is used for the detection of the K...

Anti-Kpb

FDA UDI

IMMUCOR, INC.·10888234000785·This reagent is used for the detection of the K...

Anti-Kpb

FDA UDI

AMERICAN NATIONAL RED CROSS·00858400005039·Blood Grouping Reagent

75H - KGP - 2-Shelf Cabinet

FDA UDI

Certified Safety Manufacturing, Inc.·00766588070407·75H - KGP - 2-Shelf Cabinet

FDA Pre-Market Approval

600 SERIES DYE MODULES (MODELS 630 AND 630 XP) AND SERIES 700 AND 800 KTP/532 AND KTP/YAG SURGICAL LASERS

FDA Pre-Market Approval

600 SERIES DYE MODULES (MODELS 630 AND 630 XP) AND SERIES 700 AND 800 KTP/532 AND KTP/YAG SURGICAL LASERS

WALLACE INTRAUTERINE INSEMINATION CATHETER

FDA 510(k)

FDA Class 2 ·Dental

Nixall Antimicrobial Solutions™ Skin & Wound Hydrogel

FDA 510(k)

FDA Unclassified ·Unknown

NIXALL TM WOUND AND SKIN CARE

FDA 510(k)

FDA Unclassified ·Unknown