Atlas FDA

ALPHA-I

FDA 510(k) clearance K832642 · decided 1983-11-21

Clearance details

K-number
K832642
Device name
ALPHA-I
Applicant
Johnson Flexgroup
Decision
Substantially Equivalent
Date received
1983-08-04
Decision date
1983-11-21
Days to decision
109 days
Clearance type
Traditional
Product code
LHC
Device class
1
Regulation number
890.5950
Medical specialty
Physical Medicine
Advisory committee
Physical Medicine
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
Getinge Series Warming Cabinet (K153713)Getinge Sourcing, LLC2016-06-07
ORS-3000LD Slush Drapes, ORS-1000LD Fluid Warming Drapes (K152522)Ecolab, Inc.2016-01-15
IntraTemp Solution Warmer (K150190)Ecolab, Inc.2015-02-26
NON-STERILE ORS-400N SCOPE PILLOW WARMER DRAPE (K142173)Ecolab, Inc.2014-12-30
NON-STERILE ORS WARNING DRAPES/SLUSH+WARMER DISC-DRAPE/SLUSH+WARMER PALTE-DRAPE /FLUID WARMER DRAPE,SKIRTED (K142080)Ecolab, Inc.2014-08-28
INTRATEMP SOLUTION WARMER (K083417)C Change Surgical, LLC2009-01-13
SWC/DWC WARMING CABINETS (K080609)Mac Medical2008-06-13
C CHANGE SOLUTION WARMER (K051819)C Change Surgical, LLC2005-08-15
ORS-3000LD (K023282)O.R. Solutions, Inc.2002-11-13
1075LD HUSH-SLUSH (K023283)O.R. Solutions, Inc.2002-11-13
ORS-1000LD (K021288)O.R. Solutions, Inc.2002-06-27
WARMER 2000LD (K021289)O.R. Solutions, Inc.2002-06-26

Recalls involving this device

No recalls on record reference this clearance.