Cleared Traditional

K771036 - SHAVE PREP TRAY

K771036 is an FDA 510(k) clearance for SHAVE PREP TRAY, manufactured by Parke-Davis Co.. The device is a Class 2 General Hospital device with product code KKX cleared through the Traditional 510(k) pathway after a 34-day FDA review.

K771036 · Parke-Davis Co. · General Hospital
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Jul 1977
Decision
34d
Days
Class 2
Risk

K771036 is an FDA 510(k) clearance for the SHAVE PREP TRAY. Classified as Drape, Surgical (product code KKX), Class II - Special Controls.

Submitted by Parke-Davis Co. (Mchenry, US). The FDA issued a Cleared decision on July 14, 1977 after a review of 34 days - a notably fast clearance 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: 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 Parke-Davis Co. devices

FDA 510(k) Submission Details - K771036

510(k) Number K771036 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 10, 1977
Decision Date July 14, 1977
Days to Decision 34 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
95d faster than avg
Panel avg: 129d · This submission: 34d
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 225
Devices cleared under the same product code (KKX) and FDA review panel - the closest regulatory comparables to K771036.
DRAPING MATERIAL, COLBALT 60 STERILE
K780846 · Kimberly-Clark Corp. · Jun 1978
LEAD HAND
K772387 · Edward Weck, Inc. · Apr 1978
TOWEL, DRAPE, BOUNDARY
K780036 · Procter & Gamble Mfg. Co. · Jan 1978
HYPERALIMENTATION TRAY
K771050 · American Hospital Supply Corp. · Jul 1977
SURGICAL HEAD DRAPE, DISP.
K771136 · Procter & Gamble Mfg. Co. · Jul 1977
BARRIER O.B. PACK IV
K770560 · Surgikos, Inc. · Apr 1977