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FDA 510(k)

RANGER II M6, MODEL IN-888WNL

K-Number: K002157 · 2000-08-25

ApplicantInvacare Corp.
Decision Date2000-08-25
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

RANGER II M6, MODEL IN-888WNL is the device name listed in this FDA 510(k) record. The listed applicant is Invacare Corp.. It received FDA 510(k) clearance on 2000-08-25 under 510(k) number K002157. 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 RANGER II M6, MODEL IN-888WNL?

RANGER II M6, MODEL IN-888WNL is a medical device that received FDA 510(k) clearance on 2000-08-25. The listed applicant is Invacare Corp.. The 510(k) number is K002157.

When did RANGER II M6, MODEL IN-888WNL receive FDA 510(k) clearance?

RANGER II M6, MODEL IN-888WNL received FDA 510(k) clearance on 2000-08-25, under 510(k) number K002157.

Who is the listed applicant for RANGER II M6, MODEL IN-888WNL?

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

What is the FDA product code for RANGER II M6, MODEL IN-888WNL?

The FDA product code for RANGER II M6, MODEL IN-888WNL is 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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