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FDA 510(k)

MODEL #1555 REMOTE JOYSTICK

K-Number: K880364 · 1988-09-19

ApplicantInvacare Corp.
Decision Date1988-09-19
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MODEL #1555 REMOTE JOYSTICK is the device name listed in this FDA 510(k) record. The listed applicant is Invacare Corp.. It received FDA 510(k) clearance on 1988-09-19 under 510(k) number K880364. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL #1555 REMOTE JOYSTICK?

MODEL #1555 REMOTE JOYSTICK 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 K880364.

When did MODEL #1555 REMOTE JOYSTICK receive FDA 510(k) clearance?

MODEL #1555 REMOTE JOYSTICK received FDA 510(k) clearance on 1988-09-19, under 510(k) number K880364.

Who is the listed applicant for MODEL #1555 REMOTE JOYSTICK?

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 #1555 REMOTE JOYSTICK?

The FDA product code for MODEL #1555 REMOTE JOYSTICK is ITI.

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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.

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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.

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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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