TYMPASNOSTOMY TUBE— 510(k) K953993

Substantially Equivalent

Hampton Precision Products, Inc.

FDA 510(k) clearance K953993 for TYMPASNOSTOMY TUBE, Substantially Equivalent on 1995-09-12. Applicant: Hampton Precision Products, Inc..

Clearance details

Applicant: Hampton Precision Products, Inc.
Product code: Code ETD
Advisory panel: Ear, Nose, Throat
Date received: 1995-08-24
Decision date: 1995-09-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fenton, MO, US

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