Cleared Traditional

PAP PLUS SPECULOSCOPY COMPREHENSIVE PELVIC EXAM TRAY (K955790) - FDA 510(k) Clearance

Class II Obstetrics & Gynecology device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K955790 · Trylon Corp. · Obstetrics & Gynecology device
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Mar 1996
Decision
90d
Days
Class 2
Risk

K955790 is an FDA 510(k) clearance for the PAP PLUS SPECULOSCOPY COMPREHENSIVE PELVIC EXAM TRAY. Classified as Speculum, Vaginal, Nonmetal, Fiberoptic (product code HIC), Class II - Special Controls.

Submitted by Trylon Corp. (Monarch Beach, US). The FDA issued a Cleared decision on March 21, 1996 after a review of 90 days - within the typical 510(k) review window.

This device falls under the Obstetrics & Gynecology FDA review panel, regulated under 21 CFR 884.4530 - the FDA obstetrics and gynecology 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 Obstetrics & Gynecology review framework, consistent with the majority of Class II 510(k) submissions.

View all Trylon Corp. devices

Submission Details

510(k) Number K955790 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 22, 1995
Decision Date March 21, 1996
Days to Decision 90 days
Submission Type Traditional
Review Panel Obstetrics & Gynecology (OB)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
70d faster than avg
Panel avg: 160d · This submission: 90d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code HIC Speculum, Vaginal, Nonmetal, Fiberoptic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 884.4530
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 Obstetrics & Gynecology devices follow this clearance model.