PORTABLE ISOKINETICS 3002 ISO KANE II
K-Number: K862994 · 1986-08-20
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Device Summary
Frequently Asked Questions
What is the PORTABLE ISOKINETICS 3002 ISO KANE II?
PORTABLE ISOKINETICS 3002 ISO KANE II 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 K862994.
When did PORTABLE ISOKINETICS 3002 ISO KANE II receive FDA 510(k) clearance?
PORTABLE ISOKINETICS 3002 ISO KANE II received FDA 510(k) clearance on 1986-08-20, under 510(k) number K862994.
Who is the listed applicant for PORTABLE ISOKINETICS 3002 ISO KANE II?
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 3002 ISO KANE II?
The FDA product code for PORTABLE ISOKINETICS 3002 ISO KANE II 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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