FDA 510(k)

PATIENT TROLLEY 540

K-Number: K943529 · 1994-10-04

ApplicantMerivaara Instrumentarium Corp.

Decision Date1994-10-04

Product CodeFPO

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

PATIENT TROLLEY 540 is the device name listed in this FDA 510(k) record. The listed applicant is Merivaara Instrumentarium Corp.. It received FDA 510(k) clearance on 1994-10-04 under 510(k) number K943529. 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 PATIENT TROLLEY 540?

PATIENT TROLLEY 540 is a medical device that received FDA 510(k) clearance on 1994-10-04. The listed applicant is Merivaara Instrumentarium Corp.. The 510(k) number is K943529.

When did PATIENT TROLLEY 540 receive FDA 510(k) clearance?

PATIENT TROLLEY 540 received FDA 510(k) clearance on 1994-10-04, under 510(k) number K943529.

Who is the listed applicant for PATIENT TROLLEY 540?

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

What is the FDA product code for PATIENT TROLLEY 540?

The FDA product code for PATIENT TROLLEY 540 is FPO.

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Other records listing Merivaara Instrumentarium Corp. as applicant

K944929OPTIMA DELIVERY BED (MODELS 33901, 33903, 33902, 33905)K943528PATIENT TROLLEY 545 K943262FUTURA JUNIOR 300/310

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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.