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FDA 510(k)

STRYKER 5050 STRECHAIR

K-Number: K941738 · 1994-05-06

Decision Date1994-05-06
Product CodeINM
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

STRYKER 5050 STRECHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Medical. It received FDA 510(k) clearance on 1994-05-06 under 510(k) number K941738. The device is classified under product code INM. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRYKER 5050 STRECHAIR?

STRYKER 5050 STRECHAIR is a medical device that received FDA 510(k) clearance on 1994-05-06. The listed applicant is Stryker Medical. The 510(k) number is K941738.

When did STRYKER 5050 STRECHAIR receive FDA 510(k) clearance?

STRYKER 5050 STRECHAIR received FDA 510(k) clearance on 1994-05-06, under 510(k) number K941738.

Who is the listed applicant for STRYKER 5050 STRECHAIR?

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 5050 STRECHAIR?

The FDA product code for STRYKER 5050 STRECHAIR is INM.

Related Clinical Trials

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.

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.

View all 14 devices →

Related Devices (Code: INM)

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.

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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