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FDA 510(k)

STRYKER ECLIPSE WARMING STRETCHER

K-Number: K912237 · 1991-07-30

ApplicantStryker Medical
Decision Date1991-07-30
Product CodeDWI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STRYKER ECLIPSE WARMING STRETCHER is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Medical. It received FDA 510(k) clearance on 1991-07-30 under 510(k) number K912237. The device is classified under product code DWI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRYKER ECLIPSE WARMING STRETCHER?

STRYKER ECLIPSE WARMING STRETCHER is a medical device that received FDA 510(k) clearance on 1991-07-30. The listed applicant is Stryker Medical. The 510(k) number is K912237.

When did STRYKER ECLIPSE WARMING STRETCHER receive FDA 510(k) clearance?

STRYKER ECLIPSE WARMING STRETCHER received FDA 510(k) clearance on 1991-07-30, under 510(k) number K912237.

Who is the listed applicant for STRYKER ECLIPSE WARMING STRETCHER?

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 ECLIPSE WARMING STRETCHER?

The FDA product code for STRYKER ECLIPSE WARMING STRETCHER is DWI.

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Other records listing Stryker Medical 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.

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Related Devices (Code: DWI)

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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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