Cleared Traditional

K002932 - PHACOGARD

K002932 is an FDA 510(k) clearance for PHACOGARD, manufactured by Syntec, Inc.. The device is a Class 2 Ophthalmic device with product code HQC cleared through the Traditional 510(k) pathway after a 106-day FDA review.

K002932 · Syntec, Inc. · Ophthalmic device
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Jan 2001
Decision
106d
Days
Class 2
Risk

K002932 is an FDA 510(k) clearance for the PHACOGARD. Classified as Unit, Phacofragmentation (product code HQC), Class II - Special Controls.

Submitted by Syntec, Inc. (Winfield, US). The FDA issued a Cleared decision on January 4, 2001 after a review of 106 days - within the typical 510(k) review window.

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: 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.

FDA 510(k) Submission Details - K002932

510(k) Number K002932 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 20, 2000
Decision Date January 04, 2001
Days to Decision 106 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
4d faster than avg
Panel avg: 110d · This submission: 106d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

HQC Device Classification - Class 2, Special Controls

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 258
Devices cleared under the same product code (HQC) and FDA review panel - the closest regulatory comparables to K002932.
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K002031 · Asclepion-Meditec AG · Dec 2000
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K002986 · A.R.C. Laser AG · Nov 2000
IRIS RETRACTING PHACOEMULSIFICATION SLEEVE
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K002932 · PHACOGARD
Download PDF Syntec, Inc.