Cleared Traditional

PERITRON PERINEOMETER MODEL 9300V OR 9300A (K983052) - FDA 510(k) Clearance

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

K983052 · Cardio Design Pty. , Ltd. · Gastroenterology & Urology device
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Optimized for regulatory review, auditing and printing
Oct 1998
Decision
48d
Days
Class 2
Risk

K983052 is an FDA 510(k) clearance for the PERITRON PERINEOMETER MODEL 9300V OR 9300A. Classified as Perineometer (product code HIR), Class II - Special Controls.

Submitted by Cardio Design Pty. , Ltd. (Baulkham Hills Nsw, AU). The FDA issued a Cleared decision on October 19, 1998 after a review of 48 days - a notably fast clearance cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 884.1425 - the FDA gastroenterology and urology 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 Cardio Design Pty. , Ltd. devices

Submission Details

510(k) Number K983052 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 01, 1998
Decision Date October 19, 1998
Days to Decision 48 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
82d faster than avg
Panel avg: 130d · This submission: 48d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code HIR Perineometer
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 884.1425
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 Gastroenterology & Urology devices follow this clearance model.

Regulatory Peers - HIR Perineometer

All 64
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