FDA Device Intelligence
Home › Fistula Solution Corporation › Isolation Device Mixed pack

Isolation Device Mixed pack

Fistula Solution Corporation · Model 00860013000394 · UDI-DI 00860013000394

EZS
1
510(k) clearances
49
Adverse events
0
Recalls
32
Facilities

Description

Convenience kit containing 1 each: • REF 00860013000301 Wound Crown® • REF 00860013000325 Fistula Funnel® • REF 00860013000318 Isolator Strip®

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.