TECNOL SECURE-ALL PELVIC TRACTION BELT
K-Number: K882640 · 1988-07-27
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Device Summary
Frequently Asked Questions
What is the TECNOL SECURE-ALL PELVIC TRACTION BELT?
TECNOL SECURE-ALL PELVIC TRACTION BELT is a medical device that received FDA 510(k) clearance on 1988-07-27. The listed applicant is Tecnol New Jersey Wound Care, Inc.. The 510(k) number is K882640.
When did TECNOL SECURE-ALL PELVIC TRACTION BELT receive FDA 510(k) clearance?
TECNOL SECURE-ALL PELVIC TRACTION BELT received FDA 510(k) clearance on 1988-07-27, under 510(k) number K882640.
Who is the listed applicant for TECNOL SECURE-ALL PELVIC TRACTION BELT?
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 SECURE-ALL PELVIC TRACTION BELT?
The FDA product code for TECNOL SECURE-ALL PELVIC TRACTION BELT is KQZ.
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: KQZ)
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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