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FDA 510(k)

ARROW MICRO COMPUTER CONTROL

K-Number: K885212 · 1989-03-15

Decision Date1989-03-15
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ARROW MICRO COMPUTER CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Invacare Corp.. It received FDA 510(k) clearance on 1989-03-15 under 510(k) number K885212. 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 ARROW MICRO COMPUTER CONTROL?

ARROW MICRO COMPUTER CONTROL is a medical device that received FDA 510(k) clearance on 1989-03-15. The listed applicant is Invacare Corp.. The 510(k) number is K885212.

When did ARROW MICRO COMPUTER CONTROL receive FDA 510(k) clearance?

ARROW MICRO COMPUTER CONTROL received FDA 510(k) clearance on 1989-03-15, under 510(k) number K885212.

Who is the listed applicant for ARROW MICRO COMPUTER CONTROL?

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 ARROW MICRO COMPUTER CONTROL?

The FDA product code for ARROW MICRO COMPUTER CONTROL 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.

View all 111 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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