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FDA 510(k)

WHEELCHAIR BCW 6000

K-Number: K883034 · 1988-08-02

ApplicantO'Tec Corp.
Decision Date1988-08-02
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

WHEELCHAIR BCW 6000 is the device name listed in this FDA 510(k) record. The listed applicant is O'Tec Corp.. It received FDA 510(k) clearance on 1988-08-02 under 510(k) number K883034. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WHEELCHAIR BCW 6000?

WHEELCHAIR BCW 6000 is a medical device that received FDA 510(k) clearance on 1988-08-02. The listed applicant is O'Tec Corp.. The 510(k) number is K883034.

When did WHEELCHAIR BCW 6000 receive FDA 510(k) clearance?

WHEELCHAIR BCW 6000 received FDA 510(k) clearance on 1988-08-02, under 510(k) number K883034.

Who is the listed applicant for WHEELCHAIR BCW 6000?

The FDA 510(k) record lists O'Tec Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WHEELCHAIR BCW 6000?

The FDA product code for WHEELCHAIR BCW 6000 is IOR.

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Other records listing O'Tec Corp. as applicant

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Related Devices (Code: IOR)

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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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