Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by BOB KATZ
FDA 510(k) Number
Submission Date
Device Name
Applicant
K011046
04/06/2001
AUTOPULSE, MODEL 100
REVIVANT CORP.
K040453
02/23/2004
AUTOPULSE RESUSCITATION SYSTEM, MODEL 100
REVIVANT CORP.
K032852
09/12/2003
MODIFICATION TO: AUTOPULSE RESUSCITATION SYSTEM MODEL 100
REVIVANT CORP.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact