Atlas FDA

PROSPECT GIARDIA CONTROLS

FDA 510(k) clearance K922675 · decided 1992-09-11

Clearance details

K-number
K922675
Device name
PROSPECT GIARDIA CONTROLS
Applicant
Alexon, Inc.
Decision
Substantially Equivalent
Date received
1992-06-04
Decision date
1992-09-11
Days to decision
99 days
Clearance type
Traditional
Product code
MHI
Device class
2
Regulation number
866.3220
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Mountain View, CA, 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
UNIGOLD GIARDIA (K120001)Trinity Biotech2013-03-01
GIARDIA/ CRYPTOSPORIDIUM QUIK CHEK (K103673)Techlab Inc., Corporate Research Center2011-08-18
GIARDIA FECAL ANTIGEN DETECTION LATERAL FLOW KIT, MODEL GL-LF (K081064)Ivd Research, Inc.2009-01-14
XPECT GIARDIA LATERAL FLOW ASSAY, MODEL 2450020 (K031942)Remel, Inc.2003-11-18
XPECT GIARDIA/CRYPTOSPORIDIUM LATERAL FLOW ASSAY (K031834)Remel, Inc.2003-11-10
GIARDIA II (K033274)Techlab, Inc.2003-11-04
IVD CRYPTO/GIARDIA DFA (K024113)Ivd Research, Inc.2003-03-05
IVD GIARDIA ANTIGEN DETECTION ASSAY MODEL GL-96 (K020583)Ivd Research, Inc.2002-09-17
GIARDIA/CRYPTOSPORIDIUM COMBO RAPID ASSAY (K983399)Genzyme Diagnostics1999-01-11
PREMIER GIARDIA (K982711)Meridian Diagnostics, Inc.1998-11-25
TRIAGE,PARASITE PANEL, TRIAGE CRYPTOSPORIDIUM AND ENTAMOEBA HISTOLYTICA, TRIAGE CRYPTOSPORIDIUM AND GIARDIA LAMBLIA (K982245)Biosite Incorporated1998-10-06
GIARDIA CELISA (K963135)Techlab, Inc.1996-11-29

Recalls involving this device

No recalls on record reference this clearance.