Cleared Traditional

K980295 - OPHTHAVISION IMAGING SYSTEM

K980295 is an FDA 510(k) clearance for OPHTHAVISION IMAGING SYSTEM, manufactured by Mrp Group, Inc.. The device is a Class 2 Ophthalmic device with product code HKI cleared through the Traditional 510(k) pathway after a 112-day FDA review.

K980295 · Mrp Group, Inc. · Ophthalmic device
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May 1998
Decision
112d
Days
Class 2
Risk

K980295 is an FDA 510(k) clearance for the OPHTHAVISION IMAGING SYSTEM. Classified as Camera, Ophthalmic, Ac-powered (product code HKI), Class II - Special Controls.

Submitted by Mrp Group, Inc. (Haverhill, US). The FDA issued a Cleared decision on May 19, 1998 after a review of 112 days - within the typical 510(k) review window.

This device falls under the Ophthalmic FDA review panel, regulated under 21 CFR 886.1120 - the FDA ophthalmic 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 Ophthalmic review framework, consistent with the majority of Class II 510(k) submissions.

View all Mrp Group, Inc. devices

FDA 510(k) Submission Details - K980295

510(k) Number K980295 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 27, 1998
Decision Date May 19, 1998
Days to Decision 112 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
2d slower than avg
Panel avg: 110d · This submission: 112d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

HKI Device Classification - Class 2, Special Controls

Product Code HKI Camera, Ophthalmic, Ac-powered
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 886.1120
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 Ophthalmic devices follow this clearance model.

Regulatory Peers - HKI Camera, Ophthalmic, Ac-powered

All 80
Devices cleared under the same product code (HKI) and FDA review panel - the closest regulatory comparables to K980295.
CANON NON-MYDRIATIC RETINAL CAMERA, MODEL CR-DGI
K031629 · Canon USA, Inc. · Jun 2003
NON-MYDRIATIC FUNDUS CAMERA, MODEL NM-1000
K014274 · Nidek, Inc. · Apr 2002
DISCAM DIGITAL IMAGING SYSTEM
K974535 · Marcher Enterprises, Ltd. · Aug 1998
NON-MYDRIATIC RETINAL CAMERA, MODEL CR6-45NM
K980246 · Canon USA, Inc. · May 1998
KONAN NONCON ROBO PACHY SPECULAR MICROSCOPE AND OPTICL PACHYMETER
K980357 · Konan, Inc. · Apr 1998
RETINAL CUBE
K973950 · Applied Spectral Imaging , Ltd. · Dec 1997