Atlas FDA

ALLERGEAZE PATCH TEST CHAMBERS

FDA 510(k) clearance K063160 · decided 2006-12-22

Clearance details

K-number
K063160
Device name
ALLERGEAZE PATCH TEST CHAMBERS
Applicant
Smartpractice
Decision
Substantially Equivalent
Date received
2006-10-17
Decision date
2006-12-22
Days to decision
66 days
Clearance type
Traditional
Product code
KXF
Device class
1
Regulation number
880.6025
Medical specialty
General Hospital
Advisory committee
General Hospital
Location
Phoenix, AZ, 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
FINN CHAMBERS AQUA (K123184)Smartpractice2012-12-19
ALLERGEAZE R CLEAR (K103409)Smartpractice2011-03-15
FINN CHAMBER (R) (K013820)Epitest Ltd. OY2002-01-30
IQ CHAMBERS (K992553)Dormer Laboratories, Inc.2000-04-12
EAR APPLICATOR, CATALOG NO. 2229 (K870762)Treace Medical, Inc.1987-03-06
COTTON TIPPED APPLICATORS, SINGLE (K843720)Abco Dealers, Inc.1984-10-04
COTTON SWABS (K820962)Dafoe & Dafoe, Inc.1982-04-20
FARRORS TMJ CASSETTE HOLDER (K813506)Brell Mar Products, Inc.1982-01-29
HILL TOP CHAMBER (K811365)Hill Top Research, Inc.1981-08-20
SUBCLAVIAN CATHETER INSERTION TRAY (K802580)American Pharmaseal Div. Ahsc1980-11-12
EYE APPLICATORS CAT.#980-983 (K802016)Pollak (Intl.), Ltd.1980-09-16
PREP SET CAT.#908 (K802020)Pollak (Intl.), Ltd.1980-09-09

Recalls involving this device

No recalls on record reference this clearance.