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

PULMONARY FUNCTION TESTING STS

K Number: K840741 · Decision Mar 5, 1984
Classifications
1
FEI Numbers
92
Registration Numbers
92
Same Product Code
227
Applicant Total
13
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
PULMONARY FUNCTION TESTING STS
K Number
K840741
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1840
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Circadian, Inc.
Date Received
February 1, 1984
Decision Date
March 5, 1984
Product Code
BZG
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
BZG Spirometer, Diagnostic

Similar 510(k) Clearances

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

View all

Other Clearances by Circadian, Inc.

K Number Device Name
K921878 SCANMATE III
K894956 CIRCAMED HOLTER VERSION 4
K874641 CIRCADIAN STRESS TEST II
K874155 CIRCAMED MONITOR REMOTE START CONDUCTANCE METER
K871251 CIRCAMED FULL DISCLOSURE SYSTEM
K860973 CIRCADIAN STRESS TEST SYSTEM
K851517 CIRCA MED SINGLE-CHANNEL-AMBULATORY CARDIAC MONITO
K851643 REMOTE CONTROL MODULE
K833619 CONDUCTANCE METER
K830830 CIRCA MED TWO-CHANNEL
Search all 13 clearances from Circadian, Inc. →