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

FCM 1978-02-21

CATHETERIZATION PROCEDURE TRAY

Applicant Walpak Co.

K-Number K780123

View Details →

FRG 1978-02-21

AUTOCLAVE POUCHES&ROLLS/STEAM&GAS

Applicant E.M. Adams

K-Number K780034

View Details →

FML 1978-02-21

GLOVES, FLOOR

Applicant Tillotson Rubber Co., Inc.

K-Number K780181

View Details →

IMD 1978-02-21

COLD CYCLE, CHEMICAL COLD PACK

Applicant Signal West

K-Number K780014

View Details →

FPA 1978-02-21

BURETTE INTRAVENOUS ADMIN. SETS.

Applicant Y

K-Number K780130

View Details →

FMH 1978-02-21

URINE SAMPLE COLLECTION KIT

Applicant C.R. Bard, Inc.

K-Number K780057

View Details →

ESD 1978-02-21

HEARING AID, BODY WORN

Applicant Oticon Corp.

K-Number K780197

View Details →

FCM 1978-02-21

CATHETERIZATION PROCED. TRAY, URETHRAL

Applicant Walpak Co.

K-Number K780124

View Details →

FLN 1978-02-21

PARENTERAL INFUSION CONTROLLER, ELEC.

Applicant National Patent Development Corp.

K-Number K780106

View Details →

DSK 1978-02-21

MONITOR, CARDIAC, W/BLOOD PRESS.&TEMP

Applicant Telectronics, Inc.

K-Number K772334

View Details →

GEI 1978-02-21

GENERATOR, ELECTROSURGICAL

Applicant Valleylab, Inc.

K-Number K780206

View Details →

FOZ 1978-02-21

NEEDLE CONNECTING SET, BLUNT

Applicant Abbott Laboratories

K-Number K780105

View Details →

Page 13850 of 14142

↑