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FDA 510(k)

LSPI AUTOMATIC VENTILATOR, MODEL AV3000-100

K-Number: K941871 · 1995-01-09

Decision Date1995-01-09
Product CodeBTL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LSPI AUTOMATIC VENTILATOR, MODEL AV3000-100 is the device name listed in this FDA 510(k) record. The listed applicant is Life Support Products, Inc.. It received FDA 510(k) clearance on 1995-01-09 under 510(k) number K941871. The device is classified under product code BTL. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LSPI AUTOMATIC VENTILATOR, MODEL AV3000-100?

LSPI AUTOMATIC VENTILATOR, MODEL AV3000-100 is a medical device that received FDA 510(k) clearance on 1995-01-09. The listed applicant is Life Support Products, Inc.. The 510(k) number is K941871.

When did LSPI AUTOMATIC VENTILATOR, MODEL AV3000-100 receive FDA 510(k) clearance?

LSPI AUTOMATIC VENTILATOR, MODEL AV3000-100 received FDA 510(k) clearance on 1995-01-09, under 510(k) number K941871.

Who is the listed applicant for LSPI AUTOMATIC VENTILATOR, MODEL AV3000-100?

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

What is the FDA product code for LSPI AUTOMATIC VENTILATOR, MODEL AV3000-100?

The FDA product code for LSPI AUTOMATIC VENTILATOR, MODEL AV3000-100 is BTL.

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.

Other records listing Life Support Products, Inc. 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.

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Related Devices (Code: BTL)

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.

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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