SPECTRA GUIDEWIRE INTRODUCER NEEDLE

FDA 510(k)

FDA Class 2 ·Cardiovascular

PMS PERCUTANEOUS PUNCTURE NEEDLE

FDA 510(k)

FDA Class 2 ·Cardiovascular

SureFlex HD Steerable Sheath, VersaCross HD Steerable Sheath

FDA 510(k)

FDA Class 2 ·Cardiovascular

AGILIS STEERABLE CATHETER INTRODUCER, MODEL 408304

FDA 510(k)

FDA Class 2 ·Cardiovascular

MODIFIED LABELING TO PERMANENT LEAD INTRODUCER

FDA 510(k)

FDA Class 2 ·Cardiovascular

AGILIS NXT STEERABLE INTRODUCER, MODEL G408322 AND G408323

FDA 510(k)

FDA Class 2 ·Cardiovascular

SILKPRO laser hair removal system

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

Assay, Nucleic Acid Amplification, Bacillus Anthracis

FDA classification

FDA Class 2 ·Assay, Nucleic Acid Amplification, Bacillus Anthracis

Catheter, Ureteral, Gastro-Urology

FDA classification

FDA Class 2 ·Catheter, Ureteral, Gastro-Urology

Introducer, Catheter

FDA classification

FDA Class 2 ·Introducer, Catheter

Enzyme Linked Immunoabsorbent Assay, Antibody, B. Anthracis

FDA classification

FDA Class 2 ·Enzyme Linked Immunoabsorbent Assay, Antibody, B. Anthracis

Simple In Vitro Diagnostic Device For The Detection Of Secreted Proteins From Bacillus Spp. In Human Clinical Samples

FDA classification

FDA Class 2 ·Simple In Vitro Diagnostic Device For The Detection Of Secreted Proteins From Bacillus Spp. In Human Clinical Samples

Single-Use Internal Condom

FDA Pre-Market Approval

FDA Class 2 ·REALITY FEMALE CONDOM

Monitor, Uterine Contraction, External (For Use In Clinic)

FDA Pre-Market Approval

FDA Class 2 ·GENESIS(R) HOME UTERINE ACTIVITY MONITORING SYSTEM

Single-Use Internal Condom

FDA Pre-Market Approval

FDA Class 2 ·REALITY FEMALE CONDOM

Single-Use Internal Condom

FDA Pre-Market Approval

FDA Class 2 ·REALITY FEMALE CONDOM

Single-Use Internal Condom

FDA Pre-Market Approval

FDA Class 2 ·REALITY FEMALE CONDOM

Single-Use Internal Condom

FDA Pre-Market Approval

FDA Class 2 ·REALITY FEMALE CONDOM

Single-Use Internal Condom

FDA Pre-Market Approval

FDA Class 2 ·REALITY FEMALE CONDOM

Monitor, Uterine Contraction, External (For Use In Clinic)

FDA Pre-Market Approval

FDA Class 2 ·GENESIS HOME UTERINE ACTIVITY MONITORING SYSTEM (HUAM)