Atlas FDA

O2 TEST

FDA 510(k) clearance K843847 · decided 1984-10-12

Clearance details

K-number
K843847
Device name
O2 TEST
Applicant
Erich Jaeger, Inc.
Decision
Substantially Equivalent
Date received
1984-10-01
Decision date
1984-10-12
Days to decision
11 days
Clearance type
Traditional
Product code
CCL
Device class
2
Regulation number
868.1720
Medical specialty
Anesthesiology
Advisory committee
Anesthesiology
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
PRO2 Elite Plus Oxygen Analyzer (PRO2PLUS-1) (K261389)Salter Labs2026-07-30
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Smart Check O2 (MA0236) (K250002)Life Spark Medical, LLC2025-04-24
Maxtec MaxO2 ME+p (K221734)Maxtec, LLC2023-04-01
Percent Oxygen Sensors (K213933)Careox, LLC2022-08-19
OxyMinder (K213948)Bio-Med Devices, Inc.2022-03-17
Accu O2 Oxygen Analyzer (K173807)Precision Medical, Inc.2018-05-02
MaxO2ME (K153659)Maxtec, LLC2016-06-10
CARESCAPE RESPIRATORY MODULES, E-SCO, E-SCOV, E-SCAIOV AND ACCESSORIES (K123195)GE Healthcare Finland Oy2013-02-28
ENVITEC MYSIGN O OXYGEN MEASURING DEVICE (K122290)Envitec-Wismar GmbH2013-01-23
ULTRAMAXO2 OXYGEN ANALYER (K112402)Maxtec, LLC2011-12-14
ENVITEC MEDICAL OXYGEN SENORS, MODELS OOM101; 00M102/-1;OOM103/-1/-1M;OOM104;OOM105;00M106 (K082655)Envitec-Wismar GmbH2008-11-25

Recalls involving this device

No recalls on record reference this clearance.