TECNOL VARIABLE TENSION BANDAGE
K-Number: K884440 · 1989-01-17
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Device Summary
Frequently Asked Questions
What is the TECNOL VARIABLE TENSION BANDAGE?
TECNOL VARIABLE TENSION BANDAGE is a medical device that received FDA 510(k) clearance on 1989-01-17. The listed applicant is Tecnol New Jersey Wound Care, Inc.. The 510(k) number is K884440.
When did TECNOL VARIABLE TENSION BANDAGE receive FDA 510(k) clearance?
TECNOL VARIABLE TENSION BANDAGE received FDA 510(k) clearance on 1989-01-17, under 510(k) number K884440.
Who is the listed applicant for TECNOL VARIABLE TENSION BANDAGE?
The FDA 510(k) record lists Tecnol New Jersey Wound Care, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TECNOL VARIABLE TENSION BANDAGE?
The FDA product code for TECNOL VARIABLE TENSION BANDAGE is NAD.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Tecnol New Jersey Wound Care, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: NAD)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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