Cleared Traditional

K082349 - JARIT HULKA UTERINE TENACULUM FORCEPS

K082349 is an FDA 510(k) clearance for JARIT HULKA UTERINE TENACULUM FORCEPS, manufactured by J. Jamner Surgical Instruments, Inc.. The device is a Class 2 Obstetrics & Gynecology device with product code HDC cleared through the Traditional 510(k) pathway after a 98-day FDA review.

K082349 · J. Jamner Surgical Instruments, Inc. · Obstetrics & Gynecology device
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Nov 2008
Decision
98d
Days
Class 2
Risk

K082349 is an FDA 510(k) clearance for the JARIT HULKA UTERINE TENACULUM FORCEPS. Classified as Tenaculum, Uterine (product code HDC), Class II - Special Controls.

Submitted by J. Jamner Surgical Instruments, Inc. (York, US). The FDA issued a Cleared decision on November 21, 2008 after a review of 98 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 J. Jamner Surgical Instruments, Inc. devices

FDA 510(k) Submission Details - K082349

510(k) Number K082349 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 15, 2008
Decision Date November 21, 2008
Days to Decision 98 days
Submission Type Traditional
Review Panel Obstetrics & Gynecology (OB)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
63d faster than avg
Panel avg: 161d · This submission: 98d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

HDC Device Classification - Class 2, Special Controls

Product Code HDC Tenaculum, Uterine
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.

Regulatory Peers - HDC Tenaculum, Uterine

All 13
Devices cleared under the same product code (HDC) and FDA review panel - the closest regulatory comparables to K082349.
Carevix™ Suction Cervical Stabilizer
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Bioceptive Suction Cervical Retractor
K142204 · Bioceptive, Inc. · Dec 2014
GYN DISPOSABLES TENACULUM 356T
K073182 · Gyn-Disposables, Inc. · Nov 2007
FEMTEN CERVICAL TENACULUM
K062563 · Fem Suite, LLC · May 2007
BURBANK TENACULUM
K060573 · Vascular Control Systems, Inc. · Apr 2006