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FDA 510(k)

MODEL #510/515 GENERAL TRANSPORT STRETCHER

K-Number: K895016 · 1989-09-11

ApplicantMidmark Corp.
Decision Date1989-09-11
Product CodeINW
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MODEL #510/515 GENERAL TRANSPORT STRETCHER is the device name listed in this FDA 510(k) record. The listed applicant is Midmark Corp.. It received FDA 510(k) clearance on 1989-09-11 under 510(k) number K895016. The device is classified under product code INW. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL #510/515 GENERAL TRANSPORT STRETCHER?

MODEL #510/515 GENERAL TRANSPORT STRETCHER is a medical device that received FDA 510(k) clearance on 1989-09-11. The listed applicant is Midmark Corp.. The 510(k) number is K895016.

When did MODEL #510/515 GENERAL TRANSPORT STRETCHER receive FDA 510(k) clearance?

MODEL #510/515 GENERAL TRANSPORT STRETCHER received FDA 510(k) clearance on 1989-09-11, under 510(k) number K895016.

Who is the listed applicant for MODEL #510/515 GENERAL TRANSPORT STRETCHER?

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

What is the FDA product code for MODEL #510/515 GENERAL TRANSPORT STRETCHER?

The FDA product code for MODEL #510/515 GENERAL TRANSPORT STRETCHER is INW.

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 Midmark 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.

View all 31 devices →

Related Devices (Code: INW)

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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