Atlas FDA

HEMOSITE TEST SYSTEM

FDA 510(k) clearance K994073 · decided 2000-01-14

Clearance details

K-number
K994073
Device name
HEMOSITE TEST SYSTEM
Applicant
Gds Technology, LLC
Decision
Substantially Equivalent
Date received
1999-12-02
Decision date
2000-01-14
Days to decision
43 days
Clearance type
Traditional
Product code
KHG
Device class
2
Regulation number
864.7500
Medical specialty
Hematology
Advisory committee
Hematology
Location
Elkhart, IN, 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
AnemoCheck Home (K221508)Sanguina, Inc.2023-09-29
AnemoCheck (K163215)Sanguina, LLC2017-09-13
ANEMIAPRO SELF-SCREENER (K042379)Biosafe Laboratories, Inc.2004-12-15
STAT-SITE MHGB METER, STAT-SITE MHGB METER CARD HOLDER, STAT-SITE MHGB TEST CARDS, STAT-SITE MHGB CODE WAY, MODELS 90090 (K020138)Gds Technology2002-02-11
CARESIDE HEMOGLOBIN (K001462)Careside, Inc.2000-08-21
HEMOSITE TEST SYSTEM (K973649)Gds Technology, LLC1998-08-31
ABBOTT VISION HEMOGLOBIN (MODIFICATION) (K953221)Abbott Laboratories1995-09-29
REFLOTRON HEMOGLOBIN TEST TABS (K934064)Boehringer Mannheim Corp.1993-12-06
BIOTRACK HEMOGLOBIN TEST CARTRIDGE (K895101)Biotrack, Inc.1989-10-10
CLINISTAT HEMOGLOBIN REAGENT TEST (K885227)Heraeus Kulzer, Inc.1989-02-24
FOR THE DETER. OF HEMOGLOBIN IN PLASMA #527 (K880038)Sigma Diagnostics, Inc.1988-04-21
EASY-TEST HEMOGLOBIN (HGB) ITEM #16685 (K872653)Em Diagnostic Systems, Inc.1987-07-23

Recalls involving this device

No recalls on record reference this clearance.