Atlas FDA

HELENA HBA2 QUIK COLUMN METHOD

FDA 510(k) clearance K803108 · decided 1981-01-09

Clearance details

K-number
K803108
Device name
HELENA HBA2 QUIK COLUMN METHOD
Applicant
Helena Laboratories
Decision
Substantially Equivalent
Date received
1980-12-10
Decision date
1981-01-09
Days to decision
30 days
Clearance type
Traditional
Product code
JPD
Device class
2
Regulation number
864.7400
Medical specialty
Hematology
Advisory committee
Hematology
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

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RecordFirmDate
G7 AUTOMATED HPLC ANALYZER, BETA-THALASSEMIA MODE (K020489)Tosoh Medics, Inc.2002-05-14
VARIANT II B-THALASSEMIA (K991127)Bio-Rad1999-06-10
VARIANT BETA-THALASSEMIA SHORT PROGRAM (K924122)Bio-Rad1993-03-11
GLYCOMAT GREEN HBA2 ESTIMATION REAGENT KIT (K924496)Drew Scientific , Ltd.1992-11-16
COLUMNMATE BETA THAL HBA2 CONTROL-ABNORMAL (K923317)Helena Laboratories1992-08-25
COLUMNMATE BETA-THAL HBA2 CONTROL - NORMAL (K923318)Helena Laboratories1992-08-25
COLUMNMATE(TM) BETA-THAL CAT. NO. 4515 (K913384)Helena Laboratories1991-12-17
HEMOGLOBIN A2 MICRO COLUMN TEST (K896168)Bio-Rad1990-01-18
DETER. OF HEMOGLOBIN A2 USING THE DIAMAT (K875102)Bio-Rad1988-02-24
BETA THALQUIK COLUMN #5341 (K823870)Helena Laboratories1983-02-01
HELENA SICKLE-THAL QUIK COLUMN METHOD (K812077)Helena Laboratories1981-08-18
HEMOHLOBIN A2 CONTROL-LYOPHILIZED (K801410)Isolab, Inc.1980-07-21

Recalls involving this device

No recalls on record reference this clearance.