OMNI-TRAK— 510(k) K864889

Substantially Equivalent

Invivo Research Labs, Inc.

FDA 510(k) clearance K864889 for OMNI-TRAK, Substantially Equivalent on 1987-03-06. Applicant: Invivo Research Labs, Inc.. Device class: 2.

Clearance details

Applicant
Invivo Research Labs, Inc.
Product code
Code DSB
Device class
Class 2
Regulation
21 CFR 870.2770
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Tulsa, OK, US
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