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FDA 510(k)

STS 701 TRANSPORT STRETCHER

K-Number: K933071 · 1994-01-26

Decision Date1994-01-26
Product CodeFPO
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STS 701 TRANSPORT STRETCHER is the device name listed in this FDA 510(k) record. The listed applicant is Wy'East Medical Corp.. It received FDA 510(k) clearance on 1994-01-26 under 510(k) number K933071. The device is classified under product code FPO. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STS 701 TRANSPORT STRETCHER?

STS 701 TRANSPORT STRETCHER is a medical device that received FDA 510(k) clearance on 1994-01-26. The listed applicant is Wy'East Medical Corp.. The 510(k) number is K933071.

When did STS 701 TRANSPORT STRETCHER receive FDA 510(k) clearance?

STS 701 TRANSPORT STRETCHER received FDA 510(k) clearance on 1994-01-26, under 510(k) number K933071.

Who is the listed applicant for STS 701 TRANSPORT STRETCHER?

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

What is the FDA product code for STS 701 TRANSPORT STRETCHER?

The FDA product code for STS 701 TRANSPORT STRETCHER is FPO.

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 Wy'East Medical Corp. 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.

Related Devices (Code: FPO)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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