Cleared Traditional

K874999 - PRISMA DISPOSABLE ATKINSON RETROBULBAR ...

K874999 is the FDA 510(k) clearance for PRISMA DISPOSABLE ATKINSON RETROBULBAR ... by Advanced Surgical Products, Inc.. It is a Class 1 Ophthalmic device (product code HMX) cleared through the Traditional 510(k) pathway after a 133-day FDA review.

K874999 · Advanced Surgical Products, Inc. · Ophthalmic device
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Apr 1988
Decision
133d
Days
Class 1
Risk

K874999 is an FDA 510(k) clearance for the PRISMA DISPOSABLE ATKINSON RETROBULBAR NEEDLE. Classified as Cannula, Ophthalmic (product code HMX), Class I - General Controls.

Submitted by Advanced Surgical Products, Inc. (Chesterfield, US). The FDA issued a Cleared decision on April 13, 1988 after a review of 133 days - within the typical 510(k) review window.

This device falls under the Ophthalmic FDA review panel, regulated under 21 CFR 886.4350 - 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 Advanced Surgical Products, Inc. devices

Submission Details

510(k) Number K874999 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 02, 1987
Decision Date April 13, 1988
Days to Decision 133 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
23d slower than avg
Panel avg: 110d · This submission: 133d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code HMX Cannula, Ophthalmic
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 886.4350
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.

Regulatory Peers - HMX Cannula, Ophthalmic

All 37
Devices cleared under the same product code (HMX) and FDA review panel - the closest regulatory comparables to K874999.
PRISMA DISPOS. CURVED LACHRYMAL CANNULA
K874995 · Advanced Surgical Products, Inc. · Apr 1988
PRISMA DISPOSABLE KUGLEN IRRIGATING LENS MANIPULA.
K874996 · Advanced Surgical Products, Inc. · Apr 1988
PRISMA DISPOSABLE U-SHAPED CANNULA
K874998 · Advanced Surgical Products, Inc. · Apr 1988
PRISMA DISPOSABLE VISCOELASTIC I/A CANNULA
K875002 · Advanced Surgical Products, Inc. · Apr 1988
PRISMA DISPOSABLE PUPIL CENTERING CANNULA
K875003 · Advanced Surgical Products, Inc. · Apr 1988
DISPOSABLE INFUSION CANNULA 0045-1/2/3 2.5/4.0/6.0
K873853 · Advanced Surgical Products, Inc. · Mar 1988