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FDA 510(k)

STRYKER 988 ICU BED

K-Number: K852674 · 1985-07-16

ApplicantStryker Corp.
Decision Date1985-07-16
Product CodeFNL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STRYKER 988 ICU BED is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corp.. It received FDA 510(k) clearance on 1985-07-16 under 510(k) number K852674. 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 STRYKER 988 ICU BED?

STRYKER 988 ICU BED is a medical device that received FDA 510(k) clearance on 1985-07-16. The listed applicant is Stryker Corp.. The 510(k) number is K852674.

When did STRYKER 988 ICU BED receive FDA 510(k) clearance?

STRYKER 988 ICU BED received FDA 510(k) clearance on 1985-07-16, under 510(k) number K852674.

Who is the listed applicant for STRYKER 988 ICU BED?

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

What is the FDA product code for STRYKER 988 ICU BED?

The FDA product code for STRYKER 988 ICU BED is FNL.

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Other records listing Stryker Corp. as applicant

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Related Devices (Code: FNL)

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.

K202964iBed Wireless with iBed MobileStryker CorporationK103536IBED WIRELESS WITH IBED AWARENESSStryker CorporationK982783VAIL 1000 ENCLOSED BEDVail Products, Inc.K974296MODEL 720 SERIES FULL/SEMI ELECTRIC BED 1120 FULL ELECTRIC BEDInvacare Corp.K974254BENEFIT B3--- SERIESM.C. Healthcare Products, Inc.K972115VOLKER HOSPITAL BED, MODEL K960Volker Healthcare, Inc.

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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