JAMSHIDI STYLE BIOPSY NEEDLE (ACRI) (BIOMID), ILLINOIS STYLE BIOPSY NEEDLE (ISAN)— 510(k) K952350

Name: FDA 510(k) clearance K952350
Creator: U.S. Food and Drug Administration
Published: 1995-07-17

Substantially Equivalent

Promedical , Ltd.

FDA 510(k) clearance K952350 for JAMSHIDI STYLE BIOPSY NEEDLE (ACRI) (BIOMID), ILLINOIS STYLE BIOPSY NEEDLE (ISAN), Substantially Equivalent on 1995-07-17. Applicant: Promedical , Ltd.. Device class: 2.

Clearance details

Applicant: Promedical , Ltd.
Product code: Code LWE
Device class: Class 2
Advisory panel: Unknown
Date received: 1995-05-19
Decision date: 1995-07-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wyckoff, NJ, US

Download summary PDF View on FDA.gov ↗

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