Atlas FDA

UNIVERSAL-BODYTEST

FDA 510(k) clearance K843846 · decided 1985-02-14

Clearance details

K-number
K843846
Device name
UNIVERSAL-BODYTEST
Applicant
Erich Jaeger, Inc.
Decision
Substantially Equivalent
Date received
1984-10-01
Decision date
1985-02-14
Days to decision
136 days
Clearance type
Traditional
Product code
CCM
Device class
2
Regulation number
868.1750
Medical specialty
Anesthesiology
Advisory committee
Anesthesiology
Location
Walker, MI, 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
MASTERSCREEN PAED - BABY BODY (K081823)Viasys Healthcare GmbH2009-05-18
MS PAED-BABY BODY (K023796)Erich Jaeger GmbH2003-03-03
1085 ULTIMATE E PLETHYSMOGRAPH (K943259)Medical Graphics Corp.1995-04-10
MASTERLAB PFT AND MASTERLAB BODY BOX (K893420)Quinton, Inc.1989-06-23
INFANT BODY TEST (K853390)Erich Jaeger, Inc.1986-02-05
COLLIN BODY PLETHYSMOGRAPH PLUS SYSTEM (K852102)Warren E. Collins, Inc.1985-07-31
SYSTEM 1085 BODY PLETHYSMOGRAPH (K852088)Medical Graphics Corp.1985-07-30
BODYSCREEN II (K843851)Erich Jaeger, Inc.1985-02-14
4200 PNEUMATIC MOUTH SHUTTER (K791705)Hans Rudolph, Inc.1979-10-04
CHEST BELLOWS, SMALL (K772367)Honeywell, Inc.1978-01-11

Recalls involving this device

No recalls on record reference this clearance.