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FDA 510(k)

iBed Wireless with iBed Mobile

K-Number: K202964 · 2021-06-18

ApplicantStryker Corporation
Decision Date2021-06-18
Product CodeFNL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

iBed Wireless with iBed Mobile is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corporation. It received FDA 510(k) clearance on 2021-06-18 under 510(k) number K202964. The device is classified under product code FNL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the iBed Wireless with iBed Mobile?

iBed Wireless with iBed Mobile is a medical device that received FDA 510(k) clearance on 2021-06-18. The listed applicant is Stryker Corporation. The 510(k) number is K202964.

When did iBed Wireless with iBed Mobile receive FDA 510(k) clearance?

iBed Wireless with iBed Mobile received FDA 510(k) clearance on 2021-06-18, under 510(k) number K202964.

Who is the listed applicant for iBed Wireless with iBed Mobile?

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

What is the FDA product code for iBed Wireless with iBed Mobile?

The FDA product code for iBed Wireless with iBed Mobile is FNL.

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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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