Cleared Traditional

K993804 - KSEA RIGID CULDOSCOPE AND ACCESSORIES

K993804 is an FDA 510(k) clearance for KSEA RIGID CULDOSCOPE AND ACCESSORIES, manufactured by KARL STORZ Endoscopy-America, Inc.. The device is a Class 2 Obstetrics & Gynecology device with product code HEW cleared through the Traditional 510(k) pathway after a 90-day FDA review.

K993804 · KARL STORZ Endoscopy-America, Inc. · Obstetrics & Gynecology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Feb 2000
Decision
90d
Days
Class 2
Risk

K993804 is an FDA 510(k) clearance for the KSEA RIGID CULDOSCOPE AND ACCESSORIES. Classified as Culdoscope (and Accessories) (product code HEW), Class II - Special Controls.

Submitted by KARL STORZ Endoscopy-America, Inc. (Culver City, US). The FDA issued a Cleared decision on February 7, 2000 after a review of 90 days - within the typical 510(k) review window.

This device falls under the Obstetrics & Gynecology FDA review panel, regulated under 21 CFR 884.1640 - 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 KARL STORZ Endoscopy-America, Inc. devices

FDA 510(k) Submission Details - K993804

510(k) Number K993804 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 09, 1999
Decision Date February 07, 2000
Days to Decision 90 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
70d faster than avg
Panel avg: 160d · This submission: 90d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

HEW Device Classification - Class 2, Special Controls

Product Code HEW Culdoscope (and Accessories)
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 884.1640
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 - HEW Culdoscope (and Accessories)

All 17
Devices cleared under the same product code (HEW) and FDA review panel - the closest regulatory comparables to K993804.
MCCARTNEY ACCESS TUBE
K051594 · Gynetech Pty. , Ltd. · Sep 2005
TRANSVAGINAL ENDOSCOPY SET
K033728 · KARL STORZ Endoscopy-America, Inc. · Feb 2004
FERTILOSCOPY KIT FH 1.29/FTO 1.40
K992655 · Soprane S.A. · Mar 2000
RIGID CULDOSCOPE AND ACCESSORIES
K980972 · Circon Corp. · Jun 1998
ENDOSCOPIC HYSTERECTOMY AND UTERUS MANIPULATOR
K964276 · Richard Wolf Medical Instruments Corp. · Nov 1997
KOH COLPOTOMIZER SYSTEM
K954311 · CooperSurgical, Inc. · Nov 1996