Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k) Clearances

510(k) cleared devices tracked by MedTracker

FTM 1983-08-12

SUPRAMID EXTRA SURGICAL MESH

Applicant S. Jackson, Inc.

K-Number K831723

View Details →

JPA 1983-08-12

ORTHO ABNORMAL COAGULATION LEVEL I/II

Applicant Ortho Diagnostic Systems, Inc.

K-Number K832225

View Details →

GZJ 1983-08-12

XCEL MODEL XE-1

Applicant Electrocaine Medical System

K-Number K830992

View Details →

FQO 1983-08-12

CEILING MOUNTED SUPPORT

Applicant Amsco Co.

K-Number K831086

View Details →

DXH 1983-08-12

PACELINE PATIENT TRANSMITTER MODEL 324

Applicant Pacesetter Systems

K-Number K831443

View Details →

KCW 1983-08-12

TUFCOTE EPILATION PROBE

Applicant Serapis Medical Electronics, Co.

K-Number K831048

View Details →

ITI 1983-08-12

BASE ONLY, POWER WHEELCHAIR

Applicant Intl. Medical Equipment Corp.

K-Number K832325

View Details →

DTB 1983-08-12

LIFELINE PACING LEADS #471-07 &09

Applicant Intermedics, Inc.

K-Number K832409

View Details →

KNT 1983-08-12

FEEDING TUBE PLACEMENT STYLET

Applicant Biosearch Medical Products, Inc.

K-Number K831840

View Details →

HMF 1983-08-12

ELECTRIC INSTRUMENT TABLE

Applicant CooperVision, Inc.

K-Number K832073

View Details →

DMZ 1983-08-12

PRP-1 REVERSED PHASE RESIN

Applicant Hamilton Co.

K-Number K832197

View Details →

KYD 1983-08-12

SNO STRIPS STERILE TEARFLOW TEST STRIP

Applicant Smith & Nephew, Inc.

K-Number K832181

View Details →

Page 12551 of 14156

↑