Cleared Special

K070776 - SUPRA OPHTHALMIC LASER PHOTOCOAGULATOR

K070776 is an FDA 510(k) clearance for SUPRA OPHTHALMIC LASER PHOTOCOAGULATOR, manufactured by Quantel Medical. The device is a Class 2 Ophthalmic device with product code HQF cleared through the Special 510(k) pathway after a 34-day FDA review.

K070776 · Quantel Medical · Ophthalmic device
Download Printable Device Report (PDF)
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Apr 2007
Decision
34d
Days
Class 2
Risk

K070776 is an FDA 510(k) clearance for the SUPRA OPHTHALMIC LASER PHOTOCOAGULATOR. Classified as Laser, Ophthalmic (product code HQF), Class II - Special Controls.

Submitted by Quantel Medical (Hasbrouck Heights, US). The FDA issued a Cleared decision on April 24, 2007 after a review of 34 days - a notably fast clearance cycle.

This device falls under the Ophthalmic FDA review panel, regulated under 21 CFR 886.4390 - the FDA ophthalmic device framework. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all Quantel Medical devices

FDA 510(k) Submission Details - K070776

510(k) Number K070776 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 21, 2007
Decision Date April 24, 2007
Days to Decision 34 days
Submission Type Special
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
76d faster than avg
Panel avg: 110d · This submission: 34d
Pathway characteristics
Modification to existing cleared device.

HQF Device Classification - Class 2, Special Controls

Product Code HQF Laser, Ophthalmic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 886.4390
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 - HQF Laser, Ophthalmic

All 137
Devices cleared under the same product code (HQF) and FDA review panel - the closest regulatory comparables to K070776.
SUPRA 577.Y LASER
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K050807 · Ophthalmed, LLC · Sep 2005