FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇭 Switzerland

SPIROVIT SP-2, PNEUMOCHECK II

K Number: K992823 · Decision May 12, 2000
Classifications
1
FEI Numbers
92
Registration Numbers
92
Same Product Code
227
Applicant Total
16
Review Days
263

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
SPIROVIT SP-2, PNEUMOCHECK II
K Number
K992823
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1840
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Schiller AG
Date Received
August 23, 1999
Decision Date
May 12, 2000
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 Schiller AG

K Number Device Name
K221056 ARGUS PB-3000
K183425 CARDIOVIT AT-102 G2
K170182 CARDIOVIT FT-1
K152043 Diagnostic Station DS20
K101619 WELCH ALLYN 1500 PATIENT MONITOR
K063814 BP-200 PLUS
K053207 ARGUS, MODEL LCM
K051368 BR 102 PLUS BLOOD PRESSURE HOLTER SYSTEM
K050686 CARDIOVIT AT-10PLUS
K033738 MONITORING SYSTEM, MODEL ARGUS PB-2200
Search all 16 clearances from Schiller AG →