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

EIA 1977-10-20

PERCEPTION SERIES DELIVERY SYS.

Applicant Chayes Virginia, Inc.

K-Number K771890

View Details →

EFD 1977-10-20

CAPMIX

Applicant Espe Dental Products

K-Number K771901

View Details →

DYH 1977-10-20

REPLICA ACID-ETCH

Applicant Hoyt Laboratories

K-Number K771883

View Details →

FCE 1977-10-20

ENEMA SET

Applicant Chase Mfg. Co.

K-Number K771792

View Details →

DZE 1977-10-20

EXPAND. RETENTION ENDOSSEOUS IMPLANT

Applicant A.L. Miller, Inc.

K-Number K771858

View Details →

GCP 1977-10-20

FIBEO OPTICS ILLUM. SYSTEM

Applicant Propper Mfg. Co., Inc.

K-Number K771918

View Details →

GCP 1977-10-20

FIBER OPTICS PROCTOSCOPE

Applicant Propper Mfg. Co., Inc.

K-Number K771920

View Details →

EBF 1977-10-20

REPLICA DENTAL COMPOSITE-RADIOPAQUE

Applicant Hoyt Laboratories

K-Number K771882

View Details →

EBF 1977-10-20

REPLICA DENTAL COMPOSIT

Applicant Hoyt Laboratories

K-Number K771880

View Details →

IXW 1977-10-19

AUTOMIXER, KODAK

Applicant Eastman Kodak Company

K-Number K771857

View Details →

DEN 1977-10-19

GLYCOPROTEIN TEST, LAS-R HUMAN 1-ACID

Applicant Hyland Therapeutic Div., Travenol Laboratories

K-Number K771879

View Details →

IKY 1977-10-19

MEDPRO FLOTATION SYSTEM

Applicant Medpro, Inc.

K-Number K771824

View Details →

Page 13909 of 14142

↑