PORTABLE ISOKINETICS 3004 KNEE UNIT
K-Number: K862996 · 1986-08-20
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Device Summary
Frequently Asked Questions
What is the PORTABLE ISOKINETICS 3004 KNEE UNIT?
PORTABLE ISOKINETICS 3004 KNEE UNIT is a medical device that received FDA 510(k) clearance on 1986-08-20. The listed applicant is Kent Design & Manufacturing, Inc.. The 510(k) number is K862996.
When did PORTABLE ISOKINETICS 3004 KNEE UNIT receive FDA 510(k) clearance?
PORTABLE ISOKINETICS 3004 KNEE UNIT received FDA 510(k) clearance on 1986-08-20, under 510(k) number K862996.
Who is the listed applicant for PORTABLE ISOKINETICS 3004 KNEE UNIT?
The FDA 510(k) record lists Kent Design & Manufacturing, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PORTABLE ISOKINETICS 3004 KNEE UNIT?
The FDA product code for PORTABLE ISOKINETICS 3004 KNEE UNIT is IKK.
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 Kent Design & Manufacturing, 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: IKK)
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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