ClearanceBrief
Company ยท US

Bio D Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1980 to 1980. Name variants (Inc, Corp, punctuation) are merged.

11510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
KNXCollector, Urine, (And Accessories) For Indwelling Catheter9
KMEBedding, Disposable, Medical2

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Dec 18, 1980K802739URINE COLLECTION BAG TYPE 710AP
Bio D Corp.
KNX
Dec 18, 1980K802738URINE COLLECTION BAG TYPE 1505V
Bio D Corp.
KNX
Dec 18, 1980K802737URINE COLLECTION BAG TYPE 1590V
Bio D Corp.
KNX
Dec 18, 1980K802736URINE COOLECTION BAG TYPE 2090V
Bio D Corp.
KNX
Dec 18, 1980K802735URINE COLLECTION BAG TYPE 740AP
Bio D Corp.
KNX
Dec 18, 1980K802734URINE COLLECTION BAG TYPE 710
Bio D Corp.
KNX
Dec 18, 1980K802733URINE COLLECTION BAG TYPE AP2090V
Bio D Corp.
KNX
Dec 18, 1980K802732URINE COLLECTION BAG TYPE AP2132V
Bio D Corp.
KNX
Dec 18, 1980K802729URINE COLLECTION BAG TYPE 2132V
Bio D Corp.
KNX
Dec 10, 1980K802740FLUFF UNDERPAD TYPE UP1001
Bio D Corp.
KME
Dec 10, 1980K802730FLUFF UNDERPAD TYPE UP1002
Bio D Corp.
KME

Latest recalls

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