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FDA 510(k)

C.T.M. MOBILITY SCOOTERS HS-666, HS-730, HS-570

K-Number: K000354 · 2000-08-25

Decision Date2000-08-25
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

C.T.M. MOBILITY SCOOTERS HS-666, HS-730, HS-570 is the device name listed in this FDA 510(k) record. The listed applicant is Warepalmy Enterprise, LLC (Usa). It received FDA 510(k) clearance on 2000-08-25 under 510(k) number K000354. 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 C.T.M. MOBILITY SCOOTERS HS-666, HS-730, HS-570?

C.T.M. MOBILITY SCOOTERS HS-666, HS-730, HS-570 is a medical device that received FDA 510(k) clearance on 2000-08-25. The listed applicant is Warepalmy Enterprise, LLC (Usa). The 510(k) number is K000354.

When did C.T.M. MOBILITY SCOOTERS HS-666, HS-730, HS-570 receive FDA 510(k) clearance?

C.T.M. MOBILITY SCOOTERS HS-666, HS-730, HS-570 received FDA 510(k) clearance on 2000-08-25, under 510(k) number K000354.

Who is the listed applicant for C.T.M. MOBILITY SCOOTERS HS-666, HS-730, HS-570?

The FDA 510(k) record lists Warepalmy Enterprise, LLC (Usa) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for C.T.M. MOBILITY SCOOTERS HS-666, HS-730, HS-570?

The FDA product code for C.T.M. MOBILITY SCOOTERS HS-666, HS-730, HS-570 is INI.

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 Warepalmy Enterprise, LLC (Usa) 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 7 devices →

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.

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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