ClearanceBrief
Company ยท US

Medi-Spec

FDA 510(k) clearances and medical device recalls filed under this name, 1978 to 1984. Name variants (Inc, Corp, punctuation) are merged.

8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
KKXDrape, Surgical, Antimicrobial2
GADRetractor1
GEEBrush, Biopsy, General & Plastic Surgery1
HDYDilator, Cervical, Hygroscopic-Laminaria1
HHKCurette, Suction, Endometrial (And Accessories)1
HIXMaxwell Spot, Ac-Powered1
HMPPad, Eye1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Feb 4, 1984K833068LAMINARIA JAPONICA CERVICAL DILATOR
Medi-Spec
HDY
Oct 26, 1981K812694WHISK-R
Medi-Spec
GEE
Oct 8, 1981K812426UTERINE ASPIRATION CURETTES(RIGID&FLEX)
Medi-Spec
HHK
Aug 4, 1980K801554STERILE CAST PADDING
Medi-Spec
HIX
Apr 24, 1980K800404MEDSPEC OPERATIVE OPTHALMIC KIT
Medi-Spec
HMP
Mar 12, 1980K800490STERILE DRESSING PACK
Medi-Spec
KKX
Jun 5, 1979K790952CLAMP COVERS
Medi-Spec
GAD
Aug 21, 1978K780548DISPOSA-LOOPS
Medi-Spec
KKX

Latest recalls

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