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FDA 510(k)

OSLO ARMCHAIR

K-Number: K841725 · 1984-05-09

ApplicantMondial, Inc.
Decision Date1984-05-09
Product CodeINM
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

OSLO ARMCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Mondial, Inc.. It received FDA 510(k) clearance on 1984-05-09 under 510(k) number K841725. The device is classified under product code INM. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OSLO ARMCHAIR?

OSLO ARMCHAIR is a medical device that received FDA 510(k) clearance on 1984-05-09. The listed applicant is Mondial, Inc.. The 510(k) number is K841725.

When did OSLO ARMCHAIR receive FDA 510(k) clearance?

OSLO ARMCHAIR received FDA 510(k) clearance on 1984-05-09, under 510(k) number K841725.

Who is the listed applicant for OSLO ARMCHAIR?

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

What is the FDA product code for OSLO ARMCHAIR?

The FDA product code for OSLO ARMCHAIR is INM.

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Related Devices (Code: INM)

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.

K063521NISSIN PEDIATRIC SERIES WHEELCHAIRNissin Medical, Inc.K941738STRYKER 5050 STRECHAIRStryker MedicalK941569CAREMOR CLINERWinco, Inc.K933000RECLINING GERI CHAIRS W/CASTERS & LAP TRAYWinco, Inc.K926028BENCHESTheradapt Products, Inc.K926054ELD-ARONDAK CHAIRAl'S Woodcraft, Inc.

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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