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FDA 510(k)

OPTIMA DELIVERY BED (MODELS 33901, 33903, 33902, 33905)

K-Number: K944929 · 1994-11-22

ApplicantMerivaara Instrumentarium Corp.
Decision Date1994-11-22
Product CodeFNK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

OPTIMA DELIVERY BED (MODELS 33901, 33903, 33902, 33905) 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 1994-11-22 under 510(k) number K944929. The device is classified under product code FNK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OPTIMA DELIVERY BED (MODELS 33901, 33903, 33902, 33905)?

OPTIMA DELIVERY BED (MODELS 33901, 33903, 33902, 33905) is a medical device that received FDA 510(k) clearance on 1994-11-22. The listed applicant is Merivaara Instrumentarium Corp.. The 510(k) number is K944929.

When did OPTIMA DELIVERY BED (MODELS 33901, 33903, 33902, 33905) receive FDA 510(k) clearance?

OPTIMA DELIVERY BED (MODELS 33901, 33903, 33902, 33905) received FDA 510(k) clearance on 1994-11-22, under 510(k) number K944929.

Who is the listed applicant for OPTIMA DELIVERY BED (MODELS 33901, 33903, 33902, 33905)?

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 OPTIMA DELIVERY BED (MODELS 33901, 33903, 33902, 33905)?

The FDA product code for OPTIMA DELIVERY BED (MODELS 33901, 33903, 33902, 33905) is FNK.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Merivaara Instrumentarium 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.

K943528PATIENT TROLLEY 545K943529PATIENT TROLLEY 540K943262FUTURA JUNIOR 300/310

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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