Cleared Traditional

K781952 - PAPER TAPE

K781952 is the FDA 510(k) clearance for PAPER TAPE by Johnson & Johnson Professionals, Inc.. It is a Class 1 General & Plastic Surgery device (product code FPX) cleared through the Traditional 510(k) pathway after a 16-day FDA review.

K781952 · Johnson & Johnson Professionals, Inc. · General & Plastic Surgery device
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Dec 1978
Decision
16d
Days
Class 1
Risk

K781952 is an FDA 510(k) clearance for the PAPER TAPE, HYPO ALLERGENIC. Classified as Strip, Adhesive, Closure, Skin (product code FPX), Class I - General Controls.

Submitted by Johnson & Johnson Professionals, Inc. (Raynham, US). The FDA issued a Cleared decision on December 7, 1978 after a review of 16 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 880.5240 - the FDA general and plastic surgery 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 Johnson & Johnson Professionals, Inc. devices

Submission Details

510(k) Number K781952 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 21, 1978
Decision Date December 07, 1978
Days to Decision 16 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
99d faster than avg
Panel avg: 115d · This submission: 16d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code FPX Strip, Adhesive, Closure, Skin
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 880.5240
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 - FPX Strip, Adhesive, Closure, Skin

All 19
Devices cleared under the same product code (FPX) and FDA review panel - the closest regulatory comparables to K781952.
LEUKOCLIP POROS
K792667 · Beiersdorf, Inc. · Jan 1980
HANSAPOR STERILE
K792360 · Beiersdorf, Inc. · Dec 1979
BAND AID* ADHESIVE BANDAGES
K782003 · Johnson & Johnson Professionals, Inc. · Jan 1979
SUTURELESS SKIN CLOSURE
K780565 · Abbott Laboratories · Jul 1978
CLOTH ADHESIVE TAPE
K772020 · Johnson & Johnson Professionals, Inc. · Nov 1977
POLYURETHANE PROD. FOR I.V. NEEDLES
K771125 · Devon Industries, Inc. · Aug 1977