SAUNDERS #7080 CERVICAL TRACTION SYS
K-Number: K831135 · 1983-06-24
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Device Summary
Frequently Asked Questions
What is the SAUNDERS #7080 CERVICAL TRACTION SYS?
SAUNDERS #7080 CERVICAL TRACTION SYS is a medical device that received FDA 510(k) clearance on 1983-06-24. The listed applicant is Chattanooga Group, Inc.. The 510(k) number is K831135.
When did SAUNDERS #7080 CERVICAL TRACTION SYS receive FDA 510(k) clearance?
SAUNDERS #7080 CERVICAL TRACTION SYS received FDA 510(k) clearance on 1983-06-24, under 510(k) number K831135.
Who is the listed applicant for SAUNDERS #7080 CERVICAL TRACTION SYS?
The FDA 510(k) record lists Chattanooga Group, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SAUNDERS #7080 CERVICAL TRACTION SYS?
The FDA product code for SAUNDERS #7080 CERVICAL TRACTION SYS is ILZ.
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 Chattanooga Group, 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: ILZ)
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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