Home › SONTEC INSTRUMENTS, INC. › MICRO RASPATORY
MICRO RASPATORY
SONTEC INSTRUMENTS, INC. · Model 345-266 · UDI-DI 00192896078321
KBA
Prescription
0
510(k) clearances
1
Adverse events
0
Recalls
86
Facilities
Description
MICRO RASPATORY SINGLE ENDED/SIDED 3 MILLIMETERS X 30 MILLIMETERS X 2 MILLIMETERS
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 docsData 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.
