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

ANALYZER, PULMONARY FUNCTION

K Number: K780322 · Decision Mar 14, 1978
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
89
Applicant Total
55
Review Days
15

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
ANALYZER, PULMONARY FUNCTION
K Number
K780322
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1880
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Hospal Medical Corp.
Date Received
February 27, 1978
Decision Date
March 14, 1978
Product Code
BZC
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
BZC Calculator, Pulmonary Function Data

Similar 510(k) Clearances

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

View all

Other Clearances by Hospal Medical Corp.

K Number Device Name
K893742 FILTRAL TM 20 HEMODIALYZER/FILTER
K884365 MULTIFLOW(TM) 60 KIT
K884326 FILTRAL TM 8 HEMODIALYZER
K883307 CARDIOFLOW 100 HEMOCONCENTRATOR/PREPARATION KIT
K872767 FILTRAL 10, FILTRAL 12, FILTRAL 16 HEMODIALYZER
K871218 MONITRAL S GS HEMODIALYSIS SINGLE PATIENT UNIT
K863961 HOSPAL BIOSPAL 1800S
K863592 DISSCAP 80E, 110E, 140E, 160E
K861156 HOSPAL DIALYSATE FOR CAVHD
K861230 MONITRAL S
Search all 55 clearances from Hospal Medical Corp. →