PULSE GENERATOR, CYBERLITH IMPLANTABLE— 510(k) K790221

Unknown

Intermedics, Inc.

FDA 510(k) clearance K790221 for PULSE GENERATOR, CYBERLITH IMPLANTABLE, Unknown on 1979-01-30. Applicant: Intermedics, Inc..

Clearance details

Applicant: Intermedics, Inc.
Advisory panel: Unknown
Date received: 1979-01-30
Decision date: 1979-01-30
Decision: Unknown
Clearance type: Traditional
Location: Mchenry, IL, US

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