HANDPIECE, DENTAL— 510(k) K801888

Substantially Equivalent

Aesculap Instruments Corp.

FDA 510(k) clearance K801888 for HANDPIECE, DENTAL, Substantially Equivalent on 1980-08-20. Applicant: Aesculap Instruments Corp..

Clearance details

Applicant: Aesculap Instruments Corp.
Product code: Code DZA
Advisory panel: Dental
Date received: 1980-07-28
Decision date: 1980-08-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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