FDA 510(k) Premarket Notification K993675: PEREGRINE RADIATION THERAPY DOSE CALCULATION SYSTEM

Submission Details & Decision

Normalized public record details for 510(k) notification K993675.

Source Dataset

FDA 510(k) Premarket Notifications

510(k) Number

K993675

Applicant / Sponsor

Nomos Corp.

Device Name

PEREGRINE RADIATION THERAPY DOSE CALCULATION SYSTEM

Product Code

MUJ

Decision Date

2000-09-05

Decision / Status

Substantially Equivalent (SESE)

Advisory Committee

Radiology (RA)

Clearance Type

Traditional

Third Party Flag

Date Received

1999-11-01

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