MODEL #1554 PNEUMATIC SWITCH
K-Number: K880363 · 1988-09-19
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Device Summary
Frequently Asked Questions
What is the MODEL #1554 PNEUMATIC SWITCH?
MODEL #1554 PNEUMATIC SWITCH is a medical device that received FDA 510(k) clearance on 1988-09-19. The listed applicant is Invacare Corp.. The 510(k) number is K880363.
When did MODEL #1554 PNEUMATIC SWITCH receive FDA 510(k) clearance?
MODEL #1554 PNEUMATIC SWITCH received FDA 510(k) clearance on 1988-09-19, under 510(k) number K880363.
Who is the listed applicant for MODEL #1554 PNEUMATIC SWITCH?
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 MODEL #1554 PNEUMATIC SWITCH?
The FDA product code for MODEL #1554 PNEUMATIC SWITCH 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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