Cleared Traditional

K932719 - RITTER MODEL 158 AND 159 EXAM LIGHTS

K932719 is the FDA 510(k) clearance for RITTER MODEL 158 AND 159 EXAM LIGHTS by Midmark Corp.. It is a Class 1 General Hospital device (product code KZF) cleared through the Traditional 510(k) pathway after a 181-day FDA review.

K932719 · Midmark Corp. · General Hospital
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Dec 1993
Decision
181d
Days
Class 1
Risk

K932719 is an FDA 510(k) clearance for the RITTER MODEL 158 AND 159 EXAM LIGHTS. Classified as Device, Medical Examination, Ac Powered (product code KZF), Class I - General Controls.

Submitted by Midmark Corp. (Versailles, US). The FDA issued a Cleared decision on December 2, 1993 after a review of 181 days - an extended review cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.6320 - the FDA general hospital device framework. 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 General Hospital review framework, consistent with the majority of Class II 510(k) submissions.

View all Midmark Corp. devices

Submission Details

510(k) Number K932719 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 04, 1993
Decision Date December 02, 1993
Days to Decision 181 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
52d slower than avg
Panel avg: 129d · This submission: 181d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code KZF Device, Medical Examination, Ac Powered
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 880.6320
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - KZF Device, Medical Examination, Ac Powered

All 10
Devices cleared under the same product code (KZF) and FDA review panel - the closest regulatory comparables to K932719.
WELCH ALLYN VIDEO EPISCOPE
K952835 · Welch Allyn, Inc. · Sep 1995
AC-POWERED MEDICAL EXAMINATION LIGHT
K934259 · Welch Allyn, Inc. · Jan 1994
LS100 HALOGEN EXAMINATION LIGHT, MODEL NO: 44100
K921493 · Welch Allyn, Inc. · Nov 1992
EXAMINATION LAMP
K922150 · Air-Shields, Inc. · Jul 1992
EPISCOPE, MODEL 47300
K920103 · Welch Allyn, Inc. · Apr 1992
OLYMPIC LIGHT-WARM
K896611 · Olympic Medical Corp. · Feb 1990