Cleared Traditional

K837343 - PZ-600 COMPUTERIZED AXIAL TOMOGRAPHY SCANNER

K837343 · Phoenix Medical Electronics · Radiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
May 1983
Decision
92d
Days
-
Risk

K837343 is an FDA 510(k) clearance for the PZ-600 COMPUTERIZED AXIAL TOMOGRAPHY SCANNER.

Submitted by Phoenix Medical Electronics (Chantilly, US). The FDA issued a Cleared decision on May 31, 1983 after a review of 92 days - within the typical 510(k) review window.

This device falls under the Radiology FDA review panel. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Radiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Phoenix Medical Electronics devices

FDA 510(k) Submission Details - K837343

510(k) Number K837343 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 28, 1983
Decision Date May 31, 1983
Days to Decision 92 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
15d faster than avg
Panel avg: 107d · This submission: 92d
Pathway characteristics
Predicate-based equivalence.

Device Classification - Class ,

Product Code -
Device Class -