WESCOTT TYPE BIOPSY NEEDLE— 510(k) K842406

Substantially Equivalent

Popper & Sons, Inc.

FDA 510(k) clearance K842406 for WESCOTT TYPE BIOPSY NEEDLE, Substantially Equivalent on 1984-08-09. Applicant: Popper & Sons, Inc..

Clearance details

Applicant: Popper & Sons, Inc.
Advisory panel: Unknown
Date received: 1984-06-19
Decision date: 1984-08-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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