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FDA 510(k)

GRAF CORELLO, POWERED WHEELCHAIR

K-Number: K863407 · 1986-09-23

ApplicantGraf Products, Inc.
Decision Date1986-09-23
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

GRAF CORELLO, POWERED WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Graf Products, Inc.. It received FDA 510(k) clearance on 1986-09-23 under 510(k) number K863407. 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 GRAF CORELLO, POWERED WHEELCHAIR?

GRAF CORELLO, POWERED WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1986-09-23. The listed applicant is Graf Products, Inc.. The 510(k) number is K863407.

When did GRAF CORELLO, POWERED WHEELCHAIR receive FDA 510(k) clearance?

GRAF CORELLO, POWERED WHEELCHAIR received FDA 510(k) clearance on 1986-09-23, under 510(k) number K863407.

Who is the listed applicant for GRAF CORELLO, POWERED WHEELCHAIR?

The FDA 510(k) record lists Graf Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GRAF CORELLO, POWERED WHEELCHAIR?

The FDA product code for GRAF CORELLO, POWERED WHEELCHAIR is ITI.

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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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