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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name dna-reagents, chlamydia
510(k) Number K010892
Device Name MODIFICATION HYBRID CAPTURE II CT-ID DNA TEST, MODEL 03M91-01
Applicant
DIGENE CORP.
1201 CLOPPER RD.
gaithersburg,  MD  20878
Applicant Contact mark a del vecchio
Correspondent
DIGENE CORP.
1201 CLOPPER RD.
gaithersburg,  MD  20878
Correspondent Contact mark a del vecchio
Regulation Number866.3120
Classification Product Code
LSK  
Date Received03/26/2001
Decision Date 09/24/2001
Decision substantially equivalent (SESE)
Regulation Medical Specialty Microbiology
510k Review Panel Microbiology
Type Traditional
Reviewed by Third Party No
Combination Product No
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