Cleared Traditional

K944837 - MEDICAL DEVICE TECHNOLOGIES MANUAL BIOP...

K944837 is the FDA 510(k) clearance for MEDICAL DEVICE TECHNOLOGIES MANUAL BIOP... by Medical Device Technologies, Inc.. It is a Class 2 Gastroenterology & Urology device (product code KNW) cleared through the Traditional 510(k) pathway after a 14-day FDA review.

K944837 · Medical Device Technologies, Inc. · Gastroenterology & Urology device
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Oct 1994
Decision
14d
Days
Class 2
Risk

K944837 is an FDA 510(k) clearance for the MEDICAL DEVICE TECHNOLOGIES MANUAL BIOPSY NEEDLE. Classified as Instrument, Biopsy (product code KNW), Class II - Special Controls.

Submitted by Medical Device Technologies, Inc. (Gainsville, US). The FDA issued a Cleared decision on October 14, 1994 after a review of 14 days - a notably fast clearance cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.1075 - 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 Medical Device Technologies, Inc. devices

Submission Details

510(k) Number K944837 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 30, 1994
Decision Date October 14, 1994
Days to Decision 14 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
116d faster than avg
Panel avg: 130d · This submission: 14d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code KNW Instrument, Biopsy
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.1075
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 - KNW Instrument, Biopsy

All 173
Devices cleared under the same product code (KNW) and FDA review panel - the closest regulatory comparables to K944837.
AUTOMATED TRU-CUT BIOPSY DEVICE
K954529 · Baxter Healthcare Corp · Dec 1995
URESIL INTRODUCING NEEDLE
K953923 · Uresil Corp. · Sep 1995
MANAN SUPER-CORE BIOPSY NEEDLE
K950732 · Manan Medical Products, Inc. · Mar 1995
TECHNA-CUT ASPIRATION NEEDLE
K943651 · Manan Medical Products, Inc. · Sep 1994
LIVER BIOPSY KIT
K943650 · Manan Medical Products, Inc. · Aug 1994
WANG/MILL-ROSE PLEURAL BIOPSY NEEDLE
K942630 · Mill-Rose Laboratory · Jul 1994