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FDA 510(k)

INSPIRON I.M.V. SET UP

K-Number: K760891 · 1976-12-09

ApplicantInspiron Corp.
Decision Date1976-12-09
Product CodeCBO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

INSPIRON I.M.V. SET UP is the device name listed in this FDA 510(k) record. The listed applicant is Inspiron Corp.. It received FDA 510(k) clearance on 1976-12-09 under 510(k) number K760891. The device is classified under product code CBO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSPIRON I.M.V. SET UP?

INSPIRON I.M.V. SET UP is a medical device that received FDA 510(k) clearance on 1976-12-09. The listed applicant is Inspiron Corp.. The 510(k) number is K760891.

When did INSPIRON I.M.V. SET UP receive FDA 510(k) clearance?

INSPIRON I.M.V. SET UP received FDA 510(k) clearance on 1976-12-09, under 510(k) number K760891.

Who is the listed applicant for INSPIRON I.M.V. SET UP?

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

What is the FDA product code for INSPIRON I.M.V. SET UP?

The FDA product code for INSPIRON I.M.V. SET UP is CBO.

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Other records listing Inspiron 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.

K860838INSPIRON DOUBLE SWIVEL TRACH ADAPTERK850346OXYGEN CONCENTRATORK843932VAPOR-PHASE HUMIDIFIER SYS-ADVANCEDK840935MANUAL RESUSCITATION SYSTEMK841158NEBULO 28 NEBULIZER KITK840418INSPIRATORY/EXPIRATORY MUSCLE EXERCIS

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Related Devices (Code: CBO)

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.

K811991SIMVACThe Lynn Terrell Co.K811908IMV MANIFOLDSAirlife, Inc.K791904IMV W/BAG & HOSES #M-509Mem Medical, Inc.K791912IMV FOR MONITORING #M-510Mem Medical, Inc.K791909IMV BUSHING #M-513Mem Medical, Inc.K791913IMV MANIFOLD #M-506Mem Medical, Inc.

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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