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FDA 510(k)

MODEL #520/525 ED/RECOVERY STRETCHER

K-Number: K894987 · 1989-09-05

ApplicantMedmark, Inc.
Decision Date1989-09-05
Product CodeINW
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MODEL #520/525 ED/RECOVERY STRETCHER is the device name listed in this FDA 510(k) record. The listed applicant is Medmark, Inc.. It received FDA 510(k) clearance on 1989-09-05 under 510(k) number K894987. 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 #520/525 ED/RECOVERY STRETCHER?

MODEL #520/525 ED/RECOVERY STRETCHER is a medical device that received FDA 510(k) clearance on 1989-09-05. The listed applicant is Medmark, Inc.. The 510(k) number is K894987.

When did MODEL #520/525 ED/RECOVERY STRETCHER receive FDA 510(k) clearance?

MODEL #520/525 ED/RECOVERY STRETCHER received FDA 510(k) clearance on 1989-09-05, under 510(k) number K894987.

Who is the listed applicant for MODEL #520/525 ED/RECOVERY STRETCHER?

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

What is the FDA product code for MODEL #520/525 ED/RECOVERY STRETCHER?

The FDA product code for MODEL #520/525 ED/RECOVERY 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.

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Other records listing Medmark, Inc. 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.

K914498POWDER FREE, NON-STERILE, LATEX EXAMINATION GLOVESK893949#157 EXAM LIGHT

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.

K944308JAMES LECKEY FREE STANDERJames Leckey DesignK944307JAMES LECKEY PRONE STANDERJames Leckey DesignK943974EURO TECH MARQUISE CHIROPRACTIC TABLEProgressive Electrical TherapeuticsK943975EURO TECH PLATINUM CHIROPRACTIC TABLEProgressive Electrical TherapeuticsK940238TUMBLE FORMS JUNIOR TRISTANDERCamp Intl., Inc.K932231ECONOMY HI-LOW MAT TABLE #4110 THRU 4117Bailey Mfg. Co.

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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