FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

LAUF-ERGOTEST

K Number: K843853 · Decision Nov 27, 1984
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
42
Applicant Total
28
Review Days
57

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Basic Information

Device Name
LAUF-ERGOTEST
K Number
K843853
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.5380
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Erich Jaeger, Inc.
Date Received
October 1, 1984
Decision Date
November 27, 1984
Product Code
IOL
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

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

Product Code Device Name
IOL Treadmill, Powered

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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. →