Cleared Traditional

K002961 - MINITUB MULTI-PURPOSE CASSETTES

K002961 is an FDA 510(k) clearance for MINITUB MULTI-PURPOSE CASSETTES, manufactured by Zander Medical Supplies, Inc.. The device is a Class 2 Obstetrics & Gynecology device with product code MQG cleared through the Traditional 510(k) pathway after a 60-day FDA review.

K002961 · Zander Medical Supplies, Inc. · Obstetrics & Gynecology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Nov 2000
Decision
60d
Days
Class 2
Risk

K002961 is an FDA 510(k) clearance for the MINITUB MULTI-PURPOSE CASSETTES. Classified as Accessory, Assisted Reproduction (product code MQG), Class II - Special Controls.

Submitted by Zander Medical Supplies, Inc. (Vero Beach, US). The FDA issued a Cleared decision on November 21, 2000 after a review of 60 days - a notably fast clearance cycle.

This device falls under the Obstetrics & Gynecology FDA review panel, regulated under 21 CFR 884.6120 - 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: 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 Zander Medical Supplies, Inc. devices

FDA 510(k) Submission Details - K002961

510(k) Number K002961 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 22, 2000
Decision Date November 21, 2000
Days to Decision 60 days
Submission Type Traditional
Review Panel Obstetrics & Gynecology (OB)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
100d faster than avg
Panel avg: 160d · This submission: 60d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

MQG Device Classification - Class 2, Special Controls

Product Code MQG Accessory, Assisted Reproduction
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 884.6120
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.

Regulatory Peers - MQG Accessory, Assisted Reproduction

All 22
Devices cleared under the same product code (MQG) and FDA review panel - the closest regulatory comparables to K002961.
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