Cleared Traditional

K932719 - RITTER MODEL 158 AND 159 EXAM LIGHTS

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

K932719 · Midmark Corp. · General Hospital
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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

FDA 510(k) Submission Details - K932719

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
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
52d slower than avg
Panel avg: 129d · This submission: 181d
Pathway characteristics
Predicate-based equivalence.

KZF Device Classification - Class 1, General Controls

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 14
Devices cleared under the same product code (KZF) and FDA review panel - the closest regulatory comparables to K932719.
SKYTRON EXAM LIGHT
K933564 · Skytron, Div. the Kmw Group, Inc. · Feb 1994
CHROMOPHARE
K935832 · Berchtold Holding GmbH · Feb 1994
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