Cleared Traditional

K830270 - ISOVIS WOUND PROTECTOR

K830270 is an FDA 510(k) clearance for ISOVIS WOUND PROTECTOR, manufactured by Ritmed, Inc.. The device is a Class 2 General Hospital device with product code KKX cleared through the Traditional 510(k) pathway after a 150-day FDA review.

K830270 · Ritmed, Inc. · General Hospital
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jun 1983
Decision
150d
Days
Class 2
Risk

K830270 is an FDA 510(k) clearance for the ISOVIS WOUND PROTECTOR. Classified as Drape, Surgical (product code KKX), Class II - Special Controls.

Submitted by Ritmed, Inc. (Mchenry, US). The FDA issued a Cleared decision on June 24, 1983 after a review of 150 days - an extended review cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 878.4370 - the FDA general hospital 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 General Hospital review framework, consistent with the majority of Class II 510(k) submissions.

View all Ritmed, Inc. devices

FDA 510(k) Submission Details - K830270

510(k) Number K830270 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 25, 1983
Decision Date June 24, 1983
Days to Decision 150 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
21d slower than avg
Panel avg: 129d · This submission: 150d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KKX Device Classification - Class 2, Special Controls

Product Code KKX Drape, Surgical
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.4370
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 General Hospital devices follow this clearance model.

Regulatory Peers - KKX Drape, Surgical

All 274
Devices cleared under the same product code (KKX) and FDA review panel - the closest regulatory comparables to K830270.
SINGLE-USE SURGICAL DRAPES
K833877 · Procter & Gamble Mfg. Co. · Jan 1984
LIGHT HANDLE COVER
K832278 · Concept, Inc. · Sep 1983
ISOVIS WOUND PROTECTOR
K832874 · Ritmed, Inc. · Sep 1983
GORE-TEX BARRIER SURG. DRAPES & GOWNS
K822641 · W.L. Gore & Associates, Inc. · Jan 1983
BARRIER ANTIMICROBIAL INCISE DRAPE
K820543 · Surgikos, Inc. · Jul 1982
SURGIKOS INCISE DRAPE
K820542 · Surgikos, Inc. · Jun 1982