TONOTEST BLOOD PRESSURE DEVICE— 510(k) K790682

Unknown

Robert Bosch Corp.

FDA 510(k) clearance K790682 for TONOTEST BLOOD PRESSURE DEVICE, Unknown on 1979-04-11. Applicant: Robert Bosch Corp..

Clearance details

Applicant: Robert Bosch Corp.
Advisory panel: Unknown
Date received: 1979-04-11
Decision date: 1979-04-11
Decision: Unknown
Clearance type: Traditional
Location: Mchenry, IL, US

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