Cleared Traditional

K853883 - TUBING A VIT

K853883 is the FDA 510(k) clearance for TUBING A VIT by Medical Corp. of America. It is a Class 2 Ophthalmic device (product code HQC) cleared through the Traditional 510(k) pathway after a 19-day FDA review.

K853883 · Medical Corp. of America · Ophthalmic device
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Oct 1985
Decision
19d
Days
Class 2
Risk

K853883 is an FDA 510(k) clearance for the TUBING A VIT, VIT, FRAG PACKS & NEEDLE & CLEAN WIR. Classified as Unit, Phacofragmentation (product code HQC), Class II - Special Controls.

Submitted by Medical Corp. of America (Laguna Niguel, US). The FDA issued a Cleared decision on October 8, 1985 after a review of 19 days - a notably fast clearance cycle.

This device falls under the Ophthalmic FDA review panel, regulated under 21 CFR 886.4670 - 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Medical Corp. of America devices

Submission Details

510(k) Number K853883 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 19, 1985
Decision Date October 08, 1985
Days to Decision 19 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
91d faster than avg
Panel avg: 110d · This submission: 19d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code HQC Unit, Phacofragmentation
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 886.4670
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 - HQC Unit, Phacofragmentation

All 99
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