Cleared Traditional

K902830 - PERI-BOTTLE

K902830 is an FDA 510(k) clearance for PERI-BOTTLE, manufactured by Orion Life Systems, Inc.. The device is a Class 1 Obstetrics & Gynecology device with product code HED cleared through the Traditional 510(k) pathway after a 39-day FDA review.

K902830 · Orion Life Systems, Inc. · Obstetrics & Gynecology device
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Aug 1990
Decision
39d
Days
Class 1
Risk

K902830 is an FDA 510(k) clearance for the PERI-BOTTLE. Classified as Douche Apparatus, Vaginal, Therapeutic (product code HED), Class I - General Controls.

Submitted by Orion Life Systems, Inc. (Wheeling, US). The FDA issued a Cleared decision on August 6, 1990 after a review of 39 days - a notably fast clearance cycle.

This device falls under the Obstetrics & Gynecology FDA review panel, regulated under 21 CFR 884.5900 - 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.

FDA 510(k) Submission Details - K902830

510(k) Number K902830 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 28, 1990
Decision Date August 06, 1990
Days to Decision 39 days
Submission Type Traditional
Review Panel Obstetrics & Gynecology (OB)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
122d faster than avg
Panel avg: 161d · This submission: 39d
Pathway characteristics
Predicate-based equivalence.

HED Device Classification - Class 1, General Controls

Product Code HED Douche Apparatus, Vaginal, Therapeutic
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 884.5900
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - HED Douche Apparatus, Vaginal, Therapeutic

Devices cleared under the same product code (HED) and FDA review panel - the closest regulatory comparables to K902830.
WATER WORKS DOUCHING DEVICE
K080200 · Abbott Research Group, Inc. · Jul 2008
WORRY-REMOVER IRRIGATOR
K030056 · Corisen Group, Ltd. · Apr 2003
LA JOIE
K000736 · Goomi Ehwa, Inc. · Aug 2000
DOUCHE TRAY-DISPOS. VAGINAL TRAY W/POVID
K800954 · The Healthcare Group Laboratories, Inc. · Oct 1980
DOUCH TRAY-DISPOSABLE VAGINAL TRAY W/BEN
K800956 · The Healthcare Group Laboratories, Inc. · Oct 1980
DOUCHE UNIT-1500 ML DISP. CONTAINER
K800957 · The Healthcare Group Laboratories, Inc. · Jul 1980
K902830 · PERI-BOTTLE
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