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FDA 510(k)

POWER TILT AND RECLINE SYSTEM

K-Number: K010917 · 2001-05-15

ApplicantSunrise Medical, Inc.
Decision Date2001-05-15
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

POWER TILT AND RECLINE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Sunrise Medical, Inc.. It received FDA 510(k) clearance on 2001-05-15 under 510(k) number K010917. 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 POWER TILT AND RECLINE SYSTEM?

POWER TILT AND RECLINE SYSTEM is a medical device that received FDA 510(k) clearance on 2001-05-15. The listed applicant is Sunrise Medical, Inc.. The 510(k) number is K010917.

When did POWER TILT AND RECLINE SYSTEM receive FDA 510(k) clearance?

POWER TILT AND RECLINE SYSTEM received FDA 510(k) clearance on 2001-05-15, under 510(k) number K010917.

Who is the listed applicant for POWER TILT AND RECLINE SYSTEM?

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

What is the FDA product code for POWER TILT AND RECLINE SYSTEM?

The FDA product code for POWER TILT AND RECLINE SYSTEM is ITI.

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Related Devices (Code: ITI)

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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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