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FDA 510(k)

SPRINT (POWER DRIVE WHEELCHAIR)

K-Number: K861729 · 1986-05-27

Decision Date1986-05-27
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SPRINT (POWER DRIVE WHEELCHAIR) is the device name listed in this FDA 510(k) record. The listed applicant is Everest & Jennings, Inc.. It received FDA 510(k) clearance on 1986-05-27 under 510(k) number K861729. 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 SPRINT (POWER DRIVE WHEELCHAIR)?

SPRINT (POWER DRIVE WHEELCHAIR) is a medical device that received FDA 510(k) clearance on 1986-05-27. The listed applicant is Everest & Jennings, Inc.. The 510(k) number is K861729.

When did SPRINT (POWER DRIVE WHEELCHAIR) receive FDA 510(k) clearance?

SPRINT (POWER DRIVE WHEELCHAIR) received FDA 510(k) clearance on 1986-05-27, under 510(k) number K861729.

Who is the listed applicant for SPRINT (POWER DRIVE WHEELCHAIR)?

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

What is the FDA product code for SPRINT (POWER DRIVE WHEELCHAIR)?

The FDA product code for SPRINT (POWER DRIVE WHEELCHAIR) 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 Everest & Jennings, Inc. 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 30 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

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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