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

PNEUMOSCOPE

K Number: K852337 · Decision Jul 1, 1985
Classifications
1
FEI Numbers
92
Registration Numbers
92
Same Product Code
227
Applicant Total
28
Review Days
31

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Basic Information

Device Name
PNEUMOSCOPE
K Number
K852337
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1840
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Erich Jaeger, Inc.
Date Received
May 31, 1985
Decision Date
July 1, 1985
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

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Other Clearances by Erich Jaeger, Inc.

K Number Device Name
K000396 APNOESCREEN PRO, ALPHA SCREEN PRO
K972419 TOENNIES NEUROSCREEN SYSTEM
K960078 ASTHMA MONITOR
K933839 MASTER SCREEN PNUEMO
K932744 FLOWSCREEN
K853443 ALVEO-DIFFUSION TEST
K853409 SCREENMATE
K853390 INFANT BODY TEST
K853434 ERGO-PNEUMOTEST
K853360 N20 TEST
Search all 28 clearances from Erich Jaeger, Inc. →