PACER R 9 TREADMILL
K-Number: K893032 · 1989-07-27
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Device Summary
Frequently Asked Questions
What is the PACER R 9 TREADMILL?
PACER R 9 TREADMILL is a medical device that received FDA 510(k) clearance on 1989-07-27. The listed applicant is Pacer Industries, Inc.. The 510(k) number is K893032.
When did PACER R 9 TREADMILL receive FDA 510(k) clearance?
PACER R 9 TREADMILL received FDA 510(k) clearance on 1989-07-27, under 510(k) number K893032.
Who is the listed applicant for PACER R 9 TREADMILL?
The FDA 510(k) record lists Pacer Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PACER R 9 TREADMILL?
The FDA product code for PACER R 9 TREADMILL is IOL.
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.
Related Devices (Code: IOL)
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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