FDA 510(k)

MODEL #535 PACU STRETCHER/BED & #530 ED/TRAUMA STR

K-Number: K894335 · 1989-09-12

Decision Date1989-09-12

Product CodeFMF

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

MODEL #535 PACU STRETCHER/BED & #530 ED/TRAUMA STR is the device name listed in this FDA 510(k) record. The listed applicant is Midmark Corp.. It received FDA 510(k) clearance on 1989-09-12 under 510(k) number K894335. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL #535 PACU STRETCHER/BED & #530 ED/TRAUMA STR?

MODEL #535 PACU STRETCHER/BED & #530 ED/TRAUMA STR is a medical device that received FDA 510(k) clearance on 1989-09-12. The listed applicant is Midmark Corp.. The 510(k) number is K894335.

When did MODEL #535 PACU STRETCHER/BED & #530 ED/TRAUMA STR receive FDA 510(k) clearance?

MODEL #535 PACU STRETCHER/BED & #530 ED/TRAUMA STR received FDA 510(k) clearance on 1989-09-12, under 510(k) number K894335.

Who is the listed applicant for MODEL #535 PACU STRETCHER/BED & #530 ED/TRAUMA STR?

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 #535 PACU STRETCHER/BED & #530 ED/TRAUMA STR?

The FDA product code for MODEL #535 PACU STRETCHER/BED & #530 ED/TRAUMA STR is FMF.

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Other records listing Midmark Corp. as applicant

K122643VANTAGE MODEL V5000, V5100, V5000C, V5100C K112380CLEARVISION K090670MIDMARK M3 ULTRAFAST AUTOMATIC STERILIZER K023348MIDMARK M9 ULTRACLAVE STEAM STERILIZER K003090MIDMARK PROCENTER INSTRUMENT DELIVERY SYSTEM K992744MIDMARK M4*9 EASYCLAVE STEAM STERILIZER

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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.