Aesculap
Aesculap holds FDA 510(k) medical device clearances, first cleared 2003, most recent 2010.
Top product codes for Aesculap
Recent clearances by Aesculap
- K093649 — AESCULAP STERILCONTAINER S
- K062085 — S4 SPINAL SYSTEM
- K062510 — AESCULAP STERILCONTAINER SYSTEM
- K061135 — MINOP DISPOSABLE INTRODUCER 10F, MODEL ME010; 19F, MODEL ME019
- K043079 — BICONTACT HIP SYSTEM WITH U-CAP
- K040865 — AESCULAP STERRAD 100S COMPATABLE STERILCONTAINER
- K040191 — BICONTACT HIP STEM AND FEMORAL HEAD
- K040864 — CRANIOFIX AND CRANIOFIX2 TITANIUM CLAMP SYSTEM
- K031216 — MONOPLUS POLY-P-DIOXANONE MONOFILAMENT ABSORBABLE SURGICAL SUTURE
- K031008 — AESCULAP NEURO PATTIES, NEUROSORB 4, 6, AND 75 (GREEN & WHITE)
Data sourced from openFDA. This site is unofficial and independent of the FDA.