MENTOR STERILE SALINE MAMMARY VOLUME SIZERS— 510(k) K010709

Clearance details

Applicant

Mentor Corp.

Product code

Code MRD

Device class

Unclassified

Advisory panel

Unknown

Date received

2001-03-09

Decision date

2001-04-23

Decision

Substantially Equivalent

Clearance type

Traditional

Location

Santa Barbara, CA, US

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Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K010709.