ClearanceBrief
Company ยท US

Anatech, Ltd.

FDA 510(k) clearances and medical device recalls filed under this name, 1984 to 1988. Name variants (Inc, Corp, punctuation) are merged.

14510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
IFPFormalin, Neutral Buffered3
HYJHematoxylin2
KEMAgent, Clearing2
HYKHematoxylin Harris'S1
IGESolution, Formalin Ammonium Bromide1
IGGFormaldehyde (Formalin, Formol)1
KQCStains, Hematology1
LDXFixative, Metallic Containing1
LEBMounting Media1
PPMGeneral Purpose Reagent1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jul 28, 1988K882874ZINC FORMALIN
Anatech, Ltd.
LDX
Jul 28, 1988K882873FIELDTEX HEMATOXYLIN
Anatech, Ltd.
KQC
Jun 15, 1988K882268ZINC FORMALIN CONCENTRATE
Anatech, Ltd.
IGG
Apr 5, 1988K881282XYLENE
Anatech, Ltd.
KEM
Aug 6, 1987K872663DRY-FORM
Anatech, Ltd.
IFP
Jul 9, 1987K872500ANATECH HEMATOXYLIN-EXTRA STRENGTH
Anatech, Ltd.
HYJ
Jul 9, 1987K872499ANATECH HEMATOXYLIN-NORMAL STRENGTH
Anatech, Ltd.
HYJ
Jul 9, 1987K872498HARRIS HEMATOXYLIN
Anatech, Ltd.
HYK
Mar 31, 1987K870852NBF 10% NEUTRAL BUFFERED FORMALIN
Anatech, Ltd.
IFP
Aug 28, 1984K842940CBA FORMALIN
Anatech, Ltd.
IFP
Aug 28, 1984K842862CB FORMALIN
Anatech, Ltd.
IGE
Aug 21, 1984K842986REFRAX MOUNTING MEDIUM
Anatech, Ltd.
LEB
Aug 21, 1984K842863PRO-SOFT DEHYDRANT
Anatech, Ltd.
PPM
Aug 21, 1984K842861PRO-PAR CLEARANT
Anatech, Ltd.
KEM

Latest recalls

DateFirm and productCodeLinked 510(k)
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