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FDA 510(k)

MODEL 105 VENTILATOR

K-Number: K871448 · 1987-05-07

ApplicantDevelopmed Corp.
Decision Date1987-05-07
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MODEL 105 VENTILATOR is the device name listed in this FDA 510(k) record. The listed applicant is Developmed Corp.. It received FDA 510(k) clearance on 1987-05-07 under 510(k) number K871448. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 105 VENTILATOR?

MODEL 105 VENTILATOR is a medical device that received FDA 510(k) clearance on 1987-05-07. The listed applicant is Developmed Corp.. The 510(k) number is K871448.

When did MODEL 105 VENTILATOR receive FDA 510(k) clearance?

MODEL 105 VENTILATOR received FDA 510(k) clearance on 1987-05-07, under 510(k) number K871448.

Who is the listed applicant for MODEL 105 VENTILATOR?

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

What is the FDA product code for MODEL 105 VENTILATOR?

The FDA product code for MODEL 105 VENTILATOR is CBK.

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.

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Other records listing Developmed 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.

K910915PATIENT WARMER MODEL 100C

Related Devices (Code: CBK)

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.

K253647Evita (V800); Evita (V600)Draegerwerk AG & CO KgaaK252663Inbentus VersatileIconic Solutions by Murcia, SLK251888VPAP Pediatric Face MaskHsiner Co., Ltd.K232365Vivo 45 LSOconnell Regulatory Consultants, Inc.K252173F&P OptiNIV Hospital Vented Full Face Mask Compatible with Single-limb Circuits – Size A (ONIV117A); F&P OptiNIV Hospital Vented Full Face Mask Compatible with Single-limb Circuits – Size B (ONIV117B); F&P OptiNIV Hospital Vented Full Face Mask Compatible with Single-limb Circuits – Size C (ONIV117C); F&P OptiNIV ONIV117-F Hospital Vented Full Face Mask with optional Expiratory Filter Compatible with Single-limb Circuits - Size A (ONIV117A-F); F&P OptiNIV ONIV117-F Hospital Vented FullFisher & Paykel Healthcare, Ltd.K243767SV600, SV800 VentilatorShenzhen Mindray Bio-Medical Electronics Co., Ltd.

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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