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FDA 510(k)

STRYKER DYNAMIC MATTRESS SYSTEM (DMS) MODEL #2500

K-Number: K920526 · 1992-09-21

ApplicantStryker Medical
Decision Date1992-09-21
Product CodeIOG
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

STRYKER DYNAMIC MATTRESS SYSTEM (DMS) MODEL #2500 is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Medical. It received FDA 510(k) clearance on 1992-09-21 under 510(k) number K920526. The device is classified under product code IOG. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRYKER DYNAMIC MATTRESS SYSTEM (DMS) MODEL #2500?

STRYKER DYNAMIC MATTRESS SYSTEM (DMS) MODEL #2500 is a medical device that received FDA 510(k) clearance on 1992-09-21. The listed applicant is Stryker Medical. The 510(k) number is K920526.

When did STRYKER DYNAMIC MATTRESS SYSTEM (DMS) MODEL #2500 receive FDA 510(k) clearance?

STRYKER DYNAMIC MATTRESS SYSTEM (DMS) MODEL #2500 received FDA 510(k) clearance on 1992-09-21, under 510(k) number K920526.

Who is the listed applicant for STRYKER DYNAMIC MATTRESS SYSTEM (DMS) MODEL #2500?

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

What is the FDA product code for STRYKER DYNAMIC MATTRESS SYSTEM (DMS) MODEL #2500?

The FDA product code for STRYKER DYNAMIC MATTRESS SYSTEM (DMS) MODEL #2500 is IOG.

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Other records listing Stryker Medical as applicant

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Related Devices (Code: IOG)

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.

K801250HYDRA TRED DCMedichanics, Inc.K800251MT-10, ET-20Associated Mills, 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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