FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

MODIFIED STERILIZATION METHOD OF PTI HEART-LIFT

K Number: K893436 · Decision Jul 14, 1989
Classifications
1
FEI Numbers
313
Registration Numbers
313
Same Product Code
70
Applicant Total
19
Review Days
72

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Basic Information

Device Name
MODIFIED STERILIZATION METHOD OF PTI HEART-LIFT
K Number
K893436
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
870.4500
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Pioneering Technologies, Inc.
Date Received
May 3, 1989
Decision Date
July 14, 1989
Product Code
DWS
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DWS Instruments, Surgical, Cardiovascular

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