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FDA 510(k)

MINI CROSSER BATTERY POWERED WHEELCHAIR

K-Number: K873500 · 1988-01-19

ApplicantHeisteel DK Aps
Decision Date1988-01-19
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MINI CROSSER BATTERY POWERED WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Heisteel DK Aps. It received FDA 510(k) clearance on 1988-01-19 under 510(k) number K873500. The device is classified under product code INI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINI CROSSER BATTERY POWERED WHEELCHAIR?

MINI CROSSER BATTERY POWERED WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1988-01-19. The listed applicant is Heisteel DK Aps. The 510(k) number is K873500.

When did MINI CROSSER BATTERY POWERED WHEELCHAIR receive FDA 510(k) clearance?

MINI CROSSER BATTERY POWERED WHEELCHAIR received FDA 510(k) clearance on 1988-01-19, under 510(k) number K873500.

Who is the listed applicant for MINI CROSSER BATTERY POWERED WHEELCHAIR?

The FDA 510(k) record lists Heisteel DK Aps as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MINI CROSSER BATTERY POWERED WHEELCHAIR?

The FDA product code for MINI CROSSER BATTERY POWERED WHEELCHAIR is INI.

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Related Devices (Code: INI)

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

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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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