Tegapore Wound Contact Material, Product #563X

FDA 510(k) K890354 · 3M Company

Substantially Equivalent for Some Indications

510(k) numberK890354

Submission

Device name
Tegapore Wound Contact Material, Product #563X
Applicant
3M Company
Cottae Grove, MN, US
Received
January 24, 1989
Decision date
April 27, 1989
Decision
Substantially Equivalent for Some Indications (SN)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
NAD – Dressing, Wound, Occlusive
Device class
Class I (low risk)
Regulation
21 CFR 878.4020
Specialty
General, Plastic Surgery

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Questions and answers

When was Tegapore Wound Contact Material, Product #563X cleared by the FDA?

Tegapore Wound Contact Material, Product #563X (K890354) received a 510(k) decision of Substantially Equivalent for Some Indications on April 27, 1989, 93 days after the submission was received.

What is the product code of K890354?

The FDA product code is NAD – Dressing, Wound, Occlusive, a Class I (low risk) device regulated under 21 CFR 878.4020.