ClearanceBrief
Company ยท US

Martell Medical Products, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1981 to 1995. 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
FMFSyringe, Piston4
CBTArterial Blood Sampling Kit2
JKATubes, Vials, Systems, Serum Separators, Blood Collection1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Apr 14, 1995K945454LEUR TIP CAP, VLT CAP(TM)
Martell Medical Products, Inc.
JKA
Dec 5, 1994K944941PISTON SYRINGE
Martell Medical Products, Inc.
CBT
Jul 6, 1984K841810MARK5 ARTERIAL BLOOD GAS KIT
Martell Medical Products, Inc.
FMF
Oct 21, 1982K822786MDM ARTERIAL BLOOD GAS KIT
Martell Medical Products, Inc.
CBT
Sep 28, 1982K822760ARTERIAL LINE KIT
Martell Medical Products, Inc.
FMF
May 14, 1982K821096A-LINER
Martell Medical Products, Inc.
FMF
Oct 9, 1981K812560MDM ARTERIAL BLOOD GAS SYRINGE
Martell Medical Products, Inc.
FMF

Latest recalls

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