FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

DRI-LYTE

K Number: K780353 · Decision Apr 5, 1978
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
122
Applicant Total
92
Review Days
33

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
DRI-LYTE
K Number
K780353
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5820
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Mallinckrodt Critical Care
Date Received
March 3, 1978
Decision Date
April 5, 1978
Product Code
KPO
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
KPO Dialysate Concentrate For Hemodialysis (Liquid Or Powder)

Similar 510(k) Clearances

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

View all

Other Clearances by Mallinckrodt Critical Care

K Number Device Name
K880343 BURNEY GALLBLADDER CATHETER KIT
K874605 HI-LO TEMP(R) MYOCARDIAL TEMPERATURE SENSOR
K874514 HI-LO TEMP(R) GENERAL PURPOSE TEMPERATURE PROBE
K874568 HI-LO TEMP(R) MODEL 8700 PATIENT TEMP MONITOR
K874404 HI-LO TEMP(R) SKIN TEMPERATURE SENSOR
K873461 LASER-FLEX(TM) TRACHEAL TUBE (CUFFED)
K873833 THERMOCOUPLE ADAPTER
K873004 GUIDING CATHETER
K871204 CUFFED TRACHEAL TUBE (MULTIPLE)
K862666 UNCUFFED LASER RESISTEANT TRACHEAL TUBE(TENTATIVE)
Search all 92 clearances from Mallinckrodt Critical Care →