Last synced on 14 November 2025 at 11:06 pm

PULSE GENERATOR, A-V SEQ.

Page Type
Cleared 510(K)
510(k) Number
K772202
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/1977
Days to Decision
20 days

PULSE GENERATOR, A-V SEQ.

Page Type
Cleared 510(K)
510(k) Number
K772202
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/1977
Days to Decision
20 days