Cleared Traditional

K820375 - PLASTIC OR GLASS MAGNIFIER

K820375 is an FDA 510(k) clearance for PLASTIC OR GLASS MAGNIFIER, manufactured by Gazelle Corp.. The device is a Class 1 Ophthalmic device with product code HJF cleared through the Traditional 510(k) pathway after a 125-day FDA review.

K820375 · Gazelle Corp. · Ophthalmic device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jun 1982
Decision
125d
Days
Class 1
Risk

K820375 is an FDA 510(k) clearance for the PLASTIC OR GLASS MAGNIFIER. Classified as Magnifier, Hand-held, Low-vision (product code HJF), Class I - General Controls.

Submitted by Gazelle Corp. (Walker, US). The FDA issued a Cleared decision on June 14, 1982 after a review of 125 days - within the typical 510(k) review window.

This device falls under the Ophthalmic FDA review panel, regulated under 21 CFR 886.5540 - 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 Gazelle Corp. devices

FDA 510(k) Submission Details - K820375

510(k) Number K820375 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 09, 1982
Decision Date June 14, 1982
Days to Decision 125 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
15d slower than avg
Panel avg: 110d · This submission: 125d
Pathway characteristics
Predicate-based equivalence.

HJF Device Classification - Class 1, General Controls

Product Code HJF Magnifier, Hand-held, Low-vision
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 886.5540
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.