FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

NEWCHILL(TM) CARDIAC INSULATOR

K Number: K892804 · Decision Jul 14, 1989
Classifications
1
FEI Numbers
313
Registration Numbers
313
Same Product Code
70
Applicant Total
12
Review Days
88

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
NEWCHILL(TM) CARDIAC INSULATOR
K Number
K892804
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
870.4500
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Acacia Laboratories, Inc.
Date Received
April 17, 1989
Decision Date
July 14, 1989
Product Code
DWS
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DWS Instruments, Surgical, Cardiovascular

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DWS), ordered by most recent decision date.

View all

Other Clearances by Acacia Laboratories, Inc.

K Number Device Name
K952419 STERIGAUZE GEL DRESSING
K952420 STERIGAUZE WET DRESSING
K951861 STERICARE WOUND CARE GEL
K952414 PREFILLED SYRINGE FOR INFLATION OF FOLEY CATHETER
K951914 HYDRACARE ABSORBENT WOUND DRESSING
K950344 HORIZON FOLEY CATHETERIZATION TRAY WITHOUT CATHETER
K913408 STERILE PLASTIC DRAPE
K901761 STERILE SUCTION TUBING SET
K892856 NEWMARK(TM) CORONARY ARTERY BYPASS GRAFT MARKERS
K884055 SURGI-TAG(TM) STERILE LABEL SETS
Search all 12 clearances from Acacia Laboratories, Inc. →