Cleared Traditional

K875241 - CIVCO SEED IMPLANT NEEDLE GUIDE

K875241 is an FDA 510(k) clearance for CIVCO SEED IMPLANT NEEDLE GUIDE, manufactured by CIVCO Medical Instruments Co., Inc.. The device is a Class 2 Radiology device with product code IYO cleared through the Traditional 510(k) pathway after a 114-day FDA review.

K875241 · CIVCO Medical Instruments Co., Inc. · Radiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Apr 1988
Decision
114d
Days
Class 2
Risk

K875241 is an FDA 510(k) clearance for the CIVCO SEED IMPLANT NEEDLE GUIDE. Classified as System, Imaging, Pulsed Echo, Ultrasonic (product code IYO), Class II - Special Controls.

Submitted by CIVCO Medical Instruments Co., Inc. (Kalona, US). The FDA issued a Cleared decision on April 14, 1988 after a review of 114 days - within the typical 510(k) review window.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1560 - the FDA radiology and imaging software oversight 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 Radiology review framework, consistent with the majority of Class II 510(k) submissions.

View all CIVCO Medical Instruments Co., Inc. devices

FDA 510(k) Submission Details - K875241

510(k) Number K875241 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 22, 1987
Decision Date April 14, 1988
Days to Decision 114 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
7d slower than avg
Panel avg: 107d · This submission: 114d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

IYO Device Classification - Class 2, Special Controls

Product Code IYO System, Imaging, Pulsed Echo, Ultrasonic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1560
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 Radiology devices follow this clearance model.

Regulatory Peers - IYO System, Imaging, Pulsed Echo, Ultrasonic

All 651
Devices cleared under the same product code (IYO) and FDA review panel - the closest regulatory comparables to K875241.
TRANS/R NEEDLE GUIDE
K875128 · CIVCO Medical Instruments Co., Inc. · Apr 1988
TRANS/P NEEDLE GUIDE
K875236 · CIVCO Medical Instruments Co., Inc. · Apr 1988
TRANS/V NEEDLE GUIDE
K875240 · CIVCO Medical Instruments Co., Inc. · Apr 1988
TEKNAR PROSCAN ACCESSORY PROBE
K880659 · Teknar, Inc. · Apr 1988
TRANSRECTAL PROBE BD65S-TR
K880219 · Elscint, Inc. · Mar 1988
SDR 3500 (PHILIPS PLATINUM +)
K873937 · Philips Ultrasound, Inc. · Mar 1988