PATIENT GUIDED KNEE EXERCISER
K-Number: K820120 · 1982-01-29
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Device Summary
Frequently Asked Questions
What is the PATIENT GUIDED KNEE EXERCISER?
PATIENT GUIDED KNEE EXERCISER is a medical device that received FDA 510(k) clearance on 1982-01-29. The listed applicant is Richard'S Medical Equip., Inc.. The 510(k) number is K820120.
When did PATIENT GUIDED KNEE EXERCISER receive FDA 510(k) clearance?
PATIENT GUIDED KNEE EXERCISER received FDA 510(k) clearance on 1982-01-29, under 510(k) number K820120.
Who is the listed applicant for PATIENT GUIDED KNEE EXERCISER?
The FDA 510(k) record lists Richard'S Medical Equip., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PATIENT GUIDED KNEE EXERCISER?
The FDA product code for PATIENT GUIDED KNEE EXERCISER is BXB.
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 Richard'S Medical Equip., 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: BXB)
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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