FLUFF UNDERPAD TYPE UP1001— 510(k) K802740

Substantially Equivalent

Bio D Corp.

FDA 510(k) clearance K802740 for FLUFF UNDERPAD TYPE UP1001, Substantially Equivalent on 1980-12-10. Applicant: Bio D Corp.. Device class: 1.

Clearance details

Applicant
Bio D Corp.
Product code
Code KME
Device class
Class 1
Regulation
21 CFR 880.6060
Advisory panel
General Hospital
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Mchenry, IL, US
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