ClearanceBrief
Company ยท US

Heyer Schulte Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1976 to 1979. Name variants (Inc, Corp, punctuation) are merged.

9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
JXGShunt, Central Nervous System And Components3
LCJTissue Expander And Accessories2
FMINeedle, Hypodermic, Single Lumen1
GAZTubing, Noninvasive1
GCYApparatus, Suction, Single Patient Use, Portable, Nonpowered1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Nov 16, 1979K7920962 FR KELMAN CHAMBER MAINTAINER
Heyer Schulte Corp.
FMI
Aug 3, 1979K790842SUBCUTANEOUS TISSUE EXPANDER
Heyer Schulte Corp.
LCJ
Sep 7, 1978K780706LUMBAR NERVE ROOT SHIELD
Heyer Schulte Corp.
Apr 18, 1978K780417ASEPTIC TRANSFER SET
Heyer Schulte Corp.
GAZ
Oct 11, 1977K771224RADOVAN SUBCUTANEOUS TISSUE EXPANDER
Heyer Schulte Corp.
LCJ
Nov 3, 1976K760778T-TUBE DRAIN, ROUND
Heyer Schulte Corp.
GCY
Nov 1, 1976K760785MISHLER 2 CHAMB FLUSHING VALVE,ANTI-SYPH
Heyer Schulte Corp.
JXG
Nov 1, 1976K760784MISHLER 2 CHAMB FLUSHING VALVE,STAND
Heyer Schulte Corp.
JXG
Aug 30, 1976K760501VALVE, STANDARD MODEL PUDENZE FLUSHING
Heyer Schulte Corp.
JXG

Latest recalls

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