Atlas FDA

QUALTURE

FDA 510(k) clearance K903470 · decided 1990-12-13

Clearance details

K-number
K903470
Device name
QUALTURE
Applicant
Future Medical Technologies Intl., Inc.
Decision
Substantially Equivalent
Date received
1990-08-01
Decision date
1990-12-13
Days to decision
134 days
Clearance type
Traditional
Product code
JXA
Device class
1
Regulation number
866.2660
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Princeton, NJ, 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
OSMETECH MICROBIAL ANALYSER-URINARY TRACT INFECTION DETECTOR (OMA-UTI) (K011043)Osmetech2001-11-30
URISCREEN (K981084)Diatech Diagnostics,Inc.1998-10-07
URINE SCREENING DEVICE (K972676)Combact Diagnostic Systems , Ltd.1998-02-23
TRI-TECHIN. CUSTOM BLOOD AND/OR URINE TRANSPORT KIT (K952246)Tri-Tech, Inc.1995-06-20
MULTIPLE (IZON DBS & URINE COLLECTION KIT) (K950257)Izon Business Products, Inc.1995-04-14
MULTIPLE (IZON BLOOD & URINE COLLECTION KIT) (K950221)Izon Business Products, Inc.1995-03-21
MULTIPLE (IZON URINE COLLECTION KIT) (K950246)Izon Business Products, Inc.1995-03-21
CULTURIA MACCONKEY-MUG (K934759)Clinical Convenience Products, Inc.1994-09-09
BAC-T-SCREEN (K924218)Biomerieux Vitek, Inc.1993-02-03
DIASLIDE URINE CULTURING DEVICE (K921045)Savyon Diagnostics , Ltd.1992-09-28
URI-THREE(TM), MODIFICATION (K911846)Culture Kits, Inc.1991-10-04
RAPIDEC UR (K894805)Dms Products, Inc.1989-09-26

Recalls involving this device

No recalls on record reference this clearance.