Cleared Traditional

K021676 - CYPRESS MEDICAL PRODUCTS

K021676 is an FDA 510(k) clearance for CYPRESS MEDICAL PRODUCTS, manufactured by Cypress Medical Products, Ltd.. The device is a Class 2 Obstetrics & Gynecology device with product code HIB cleared through the Traditional 510(k) pathway after a 52-day FDA review.

K021676 · Cypress Medical Products, Ltd. · Obstetrics & Gynecology device
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Jul 2002
Decision
52d
Days
Class 2
Risk

K021676 is an FDA 510(k) clearance for the CYPRESS MEDICAL PRODUCTS, LP DISPOSABLE VAGINAL SPECULUM, NON-METAL. Classified as Speculum, Vaginal, Nonmetal (product code HIB), Class II - Special Controls.

Submitted by Cypress Medical Products, Ltd. (Mc Henry, US). The FDA issued a Cleared decision on July 12, 2002 after a review of 52 days - a notably fast clearance cycle.

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: 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 Cypress Medical Products, Ltd. devices

FDA 510(k) Submission Details - K021676

510(k) Number K021676 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 21, 2002
Decision Date July 12, 2002
Days to Decision 52 days
Submission Type Traditional
Review Panel Obstetrics & Gynecology (OB)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
108d faster than avg
Panel avg: 160d · This submission: 52d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

HIB Device Classification - Class 2, Special Controls

Product Code HIB Speculum, Vaginal, Nonmetal
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 - HIB Speculum, Vaginal, Nonmetal

All 12
Devices cleared under the same product code (HIB) and FDA review panel - the closest regulatory comparables to K021676.
SPECULUM, VAGINAL, NONMETAL
K120743 · Welch Allyn, Inc. · Mar 2012
MEDLINE DISPOSABLE VAGINAL SPECULUM
K072942 · Medline Industries, Inc. · Feb 2008
KLEENSPEC SINGLE USE VAGINAL SPECULUM AND 790 SERIES CORDLESS ILLUMINATION SYSTEM
K070964 · Welch Allyn, Inc. · May 2007
WALLACH'S ULTIMATE REUSABLE, PLASTIC VAGINAL SPECULUM
K992736 · Wallach Surgical Devices, Inc. · Sep 1999
NYLON COATED SPECULA
K925501 · Zinnanti Surgical Instruments, Inc. · Jun 1997
VERSA-VU
K951898 · CooperSurgical, Inc. · Dec 1995