Atlas FDA

MHJ

15 FDA 510(k) clearances · Product code

141 daysmedian time to decision
307 days90th percentile
15clearances measured

FDA profile

Official device name
Cryptosporidium Spp.
Device class
Class II (moderate risk)
Regulation
21 CFR 866.3220
Medical specialty
Microbiology
Adverse events (MAUDE)
2002: 2 · 2004: 2
Reports received by FDA, not confirmed device causation - volume tracks device popularity as much as risk.
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RecordFirmDate
TRI-COMBO PARASITE SCREEN (K171078)Techlab, Inc.2017-07-10
UNI-GOLD CRYPTOSPORIDIUM (K121565)Trinity Biotech2013-02-08
GIARDIA/CRYPTOSPORIDIUM CHEK (K051929)Techlab, Inc.2005-11-17
CRYPTOSPORIDIUM II (K052932)Techlab, Inc.2005-11-04
XPECT CRYPTOSPORIDIUM LATERAL FLOW ASSAY, MODEL 2451020 (K031965)Remel, Inc.2003-11-14
IVD CRYPTOSPORIDIUM ANTIGEN DETECTION ASSAY, MODEL CP-96 (K031059)Ivd Research, Inc.2003-07-10
PREMIER CRYPTOSPORIDIUM (K982764)Meridian Diagnostics, Inc.1998-12-03
MODIFICATION TO PROSPECT CRYPTOSPORIDIUM MICROTITER ASSAY (K982709)Alexon - Trend, Inc.1998-09-03
CRYPTOSPORIDIUM TEST (K980354)Techlab, Inc.1998-05-18
CRYPTO-CEL IF TEST (K955852)Techlab, Inc.1996-08-05
TREND CRYPTOSPORIDIUM DETECTION TEST SYSTEMS (K955755)Trend Scientific, Inc.1996-07-11
LMD CRYPTOSPORIDIUM ANTIGEN DETECTION (K955345)Lmd Laboratories1996-06-07
PROSPECT CRYPTOSPORIDIUM RAPID ASSAY (K936191)Alexon Biomedical, Inc.1994-11-17
PROSPECT(TM/CRYPTOSPORIDIUM (K912242)Alexon, Inc.1992-03-23
CRYPTOSPORIDIUM ANTIGEN DETECTION (K905598)Lmd Laboratories1991-09-05

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Every clearance here is in the API, with alerts when new ones post.