K790221Unknown

Pulse Generator, Cyberlith Implantable

Name: K790221 Pulse Generator, Cyberlith Implantable
Creator: Intermedics, Inc.
Published: 1979-01-30
License: https://open.fda.gov/license/

Intermedics, Inc., Mchenry IL / Traditional, Unknown

FDA source

K790221 is the FDA 510(k) clearance record for PULSE GENERATOR, CYBERLITH IMPLANTABLE, cleared for Intermedics, Inc. on 1979-01-30. FDA records list 211 510(k) clearances for Intermedics, Inc., from 1977-09-12 to 1996-12-16. As of 2026-09-10, FDA records show no recalls naming K790221.

Clearance record

Decision date: 1979-01-30
Received: 1979-01-30 (0 days to decision)
Review panel: Unknown
Applicant: Intermedics, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review: No