TILT/RECLINER FOR POWER WHEELCHAIRS, MODEL 2G
K-Number: K991119 · 1999-08-19
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Device Summary
Frequently Asked Questions
What is the TILT/RECLINER FOR POWER WHEELCHAIRS, MODEL 2G?
TILT/RECLINER FOR POWER WHEELCHAIRS, MODEL 2G is a medical device that received FDA 510(k) clearance on 1999-08-19. The listed applicant is Invacare Corp.. The 510(k) number is K991119.
When did TILT/RECLINER FOR POWER WHEELCHAIRS, MODEL 2G receive FDA 510(k) clearance?
TILT/RECLINER FOR POWER WHEELCHAIRS, MODEL 2G received FDA 510(k) clearance on 1999-08-19, under 510(k) number K991119.
Who is the listed applicant for TILT/RECLINER FOR POWER WHEELCHAIRS, MODEL 2G?
The FDA 510(k) record lists Invacare Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TILT/RECLINER FOR POWER WHEELCHAIRS, MODEL 2G?
The FDA product code for TILT/RECLINER FOR POWER WHEELCHAIRS, MODEL 2G is ITI.
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 Invacare Corp. 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: ITI)
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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