Cleared Traditional

K833800 - BEECHER 20 GA. PROBE

K833800 is an FDA 510(k) clearance for BEECHER 20 GA. PROBE, manufactured by Beecher Medical Diagnostic Instrumentation. The device is a Class 2 Ophthalmic device with product code HQC cleared through the Traditional 510(k) pathway after a 65-day FDA review.

K833800 · Beecher Medical Diagnostic Instrumentation · Ophthalmic device
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Jan 1984
Decision
65d
Days
Class 2
Risk

K833800 is an FDA 510(k) clearance for the BEECHER 20 GA. PROBE. Classified as Unit, Phacofragmentation (product code HQC), Class II - Special Controls.

Submitted by Beecher Medical Diagnostic Instrumentation (Mchenry, US). The FDA issued a Cleared decision on January 4, 1984 after a review of 65 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 Beecher Medical Diagnostic Instrumentation devices

FDA 510(k) Submission Details - K833800

510(k) Number K833800 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 31, 1983
Decision Date January 04, 1984
Days to Decision 65 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
45d faster than avg
Panel avg: 110d · This submission: 65d
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 197
Devices cleared under the same product code (HQC) and FDA review panel - the closest regulatory comparables to K833800.
DISPOSABLE I/A HANDPIECE
K833784 · CooperVision, Inc. · Feb 1984
IRRIGATION ASPIRATION KIT
K833405 · American Medical Optics · Jan 1984
STORZ EXTRA
K833064 · Storz Instrument Co. · Jan 1984
EPSILON ULTRASONIC TIP
K831836 · CooperVision, Inc. · Jun 1983
ULTRAKIT
K831172 · Staar Surgical Co. · Jun 1983
IV STAND
K830474 · Teknar, Inc. · Apr 1983