Cleared Traditional

K982300 - TRANSVIEW (TRANSMISSION SYSTEM),MODEL NDTR-701A

K982300 is an FDA 510(k) clearance for TRANSVIEW (TRANSMISSION SYSTEM), manufactured by Toshiba America Medical Systems, In.C. The device is a Class 2 Radiology device with product code KPS cleared through the Traditional 510(k) pathway after a 86-day FDA review.

K982300 · Toshiba America Medical Systems, In.C · Radiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Sep 1998
Decision
86d
Days
Class 2
Risk

K982300 is an FDA 510(k) clearance for the TRANSVIEW (TRANSMISSION SYSTEM),MODEL NDTR-701A. Classified as System, Tomography, Computed, Emission (product code KPS), Class II - Special Controls.

Submitted by Toshiba America Medical Systems, In.C (Tustin, US). The FDA issued a Cleared decision on September 25, 1998 after a review of 86 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1200 - the FDA radiology and imaging software oversight framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Toshiba America Medical Systems, In.C devices

FDA 510(k) Submission Details - K982300

510(k) Number K982300 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 01, 1998
Decision Date September 25, 1998
Days to Decision 86 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
21d faster than avg
Panel avg: 107d · This submission: 86d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KPS Device Classification - Class 2, Special Controls

Product Code KPS System, Tomography, Computed, Emission
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1200
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Radiology devices follow this clearance model.

Regulatory Peers - KPS System, Tomography, Computed, Emission

All 369
Devices cleared under the same product code (KPS) and FDA review panel - the closest regulatory comparables to K982300.
DIGIRAD 2020TC SPECT IMAGING SYSTEM
K982855 · Digirad Corp. · Nov 1998
E.CAM EXTRA HIGH ENERGY COLLIMATOR
K982387 · Siemens Medical Solutions USA, Inc. · Oct 1998
AUTOMATED MEDICAL REPORT WRITER
K981553 · Woodson and Associates, LLC · Sep 1998
HAMAMATSU PET SCANNER, MODEL SHR-22000
K982171 · Hamamatsu Photonics K.K. · Sep 1998
NUCAMMA R+
K982044 · Is2 Research, Inc. · Sep 1998
NUCAMMA RX
K982045 · Is2 Research, Inc. · Sep 1998