CUI MAMMARY PROTHESIS SIZER— 510(k) K831566

Substantially Equivalent

Cox-Uphuff Intl.

FDA 510(k) clearance K831566 for CUI MAMMARY PROTHESIS SIZER, Substantially Equivalent on 1983-08-12. Applicant: Cox-Uphuff Intl.. Device class: Unclassified.

Clearance details

Applicant
Cox-Uphuff Intl.
Product code
Code MRD
Device class
Unclassified
Advisory panel
Unknown
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Walker, MI, US
Download summary PDFView on FDA.gov ↗

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Recalls naming K831566

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K831566.

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