ClearanceBrief
Company ยท US

Anarobe Systems

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

7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
JSCCulture Media, General Nutrient Broth2
JSFCulture Media, Single Biochemical Test2
JSHCulture Media, Non-Selective And Differential2
JTZCulture Media, Antimicrobial Susceptibility Test, Mueller Hinton Agar/Broth1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Aug 17, 1984K842854MUELLER HINTON BROTH
Anarobe Systems
JTZ
Aug 17, 1984K842850TRIPLE SUGAR IRON
Anarobe Systems
JSH
Aug 7, 1984K842851ORNITHINE INDOLE MOTILITY
Anarobe Systems
JSH
Aug 3, 1984K842855CHRISTENSEN'S UREA AGAR
Anarobe Systems
JSF
Aug 3, 1984K842853LYSINE IRON AGAR
Anarobe Systems
JSF
Aug 3, 1984K842852BRAIN HEART INFUSION BROTH
Anarobe Systems
JSC
Aug 3, 1984K842849TRYPTICASE SOY BROTH
Anarobe Systems
JSC

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
Get alerts for these product codes