IMPOAID— 510(k) K000730

Substantially Equivalent

Impoaid, Inc.

FDA 510(k) clearance K000730 for IMPOAID, Substantially Equivalent on 2000-10-19. Applicant: Impoaid, Inc.. Device class: 2.

Clearance details

Applicant: Impoaid, Inc.
Product code: Code LKY
Device class: Class 2
Regulation: 21 CFR 876.5020
Advisory panel: Gastroenterology, Urology
Date received: 2000-03-06
Decision date: 2000-10-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Stillwater, MN, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LKY

K041573 — NANMA VACUUM PUMP PROXZEK MODEL 2M9498S2004-08-25
K032776 — VACURECT VACUUM CONSTRICTION DEVICE2003-10-03
K030119 — NANMA ADJUSTABLE CONSTRICTION RING2003-08-06
K030913 — NANMA VACUUM PUMP2003-06-03
K013113 — MODIFICATION TO NANMA VACUUM PUMP2002-12-20

Data sourced from openFDA. This site is unofficial and independent of the FDA.