Heyer Schulte Corp.
Heyer Schulte Corp. holds FDA 510(k) medical device clearances, first cleared 1976, most recent 1979.
Top product codes for Heyer Schulte Corp.
Recent clearances by Heyer Schulte Corp.
- K792096 — 2 FR KELMAN CHAMBER MAINTAINER
- K790842 — SUBCUTANEOUS TISSUE EXPANDER
- K780706 — LUMBAR NERVE ROOT SHIELD
- K780417 — ASEPTIC TRANSFER SET
- K771224 — RADOVAN SUBCUTANEOUS TISSUE EXPANDER
- K760778 — T-TUBE DRAIN, ROUND
- K760784 — MISHLER 2 CHAMB FLUSHING VALVE,STAND
- K760785 — MISHLER 2 CHAMB FLUSHING VALVE,ANTI-SYPH
- K760501 — VALVE, STANDARD MODEL PUDENZE FLUSHING
Data sourced from openFDA. This site is unofficial and independent of the FDA.