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FDA 510(k)

BLEASE FRONTLINE PLUS RANGE, ANESTHESIA MACHINES, MODEL 440, 560 AND 690

K-Number: K003251 · 2001-05-23

Decision Date2001-05-23
Product CodeBSZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BLEASE FRONTLINE PLUS RANGE, ANESTHESIA MACHINES, MODEL 440, 560 AND 690 is the device name listed in this FDA 510(k) record. The listed applicant is Blease Medical Equipment , Ltd.. It received FDA 510(k) clearance on 2001-05-23 under 510(k) number K003251. The device is classified under product code BSZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLEASE FRONTLINE PLUS RANGE, ANESTHESIA MACHINES, MODEL 440, 560 AND 690?

BLEASE FRONTLINE PLUS RANGE, ANESTHESIA MACHINES, MODEL 440, 560 AND 690 is a medical device that received FDA 510(k) clearance on 2001-05-23. The listed applicant is Blease Medical Equipment , Ltd.. The 510(k) number is K003251.

When did BLEASE FRONTLINE PLUS RANGE, ANESTHESIA MACHINES, MODEL 440, 560 AND 690 receive FDA 510(k) clearance?

BLEASE FRONTLINE PLUS RANGE, ANESTHESIA MACHINES, MODEL 440, 560 AND 690 received FDA 510(k) clearance on 2001-05-23, under 510(k) number K003251.

Who is the listed applicant for BLEASE FRONTLINE PLUS RANGE, ANESTHESIA MACHINES, MODEL 440, 560 AND 690?

The FDA 510(k) record lists Blease Medical Equipment , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BLEASE FRONTLINE PLUS RANGE, ANESTHESIA MACHINES, MODEL 440, 560 AND 690?

The FDA product code for BLEASE FRONTLINE PLUS RANGE, ANESTHESIA MACHINES, MODEL 440, 560 AND 690 is BSZ.

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 Blease Medical Equipment , Ltd. 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.

Related Devices (Code: BSZ)

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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