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FDA 510(k)

ANESTHESIA MACHINE

K-Number: K771057 · 1977-07-05

ApplicantForegger
Decision Date1977-07-05
Product CodeBSZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ANESTHESIA MACHINE is the device name listed in this FDA 510(k) record. The listed applicant is Foregger. It received FDA 510(k) clearance on 1977-07-05 under 510(k) number K771057. 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 ANESTHESIA MACHINE?

ANESTHESIA MACHINE is a medical device that received FDA 510(k) clearance on 1977-07-05. The listed applicant is Foregger. The 510(k) number is K771057.

When did ANESTHESIA MACHINE receive FDA 510(k) clearance?

ANESTHESIA MACHINE received FDA 510(k) clearance on 1977-07-05, under 510(k) number K771057.

Who is the listed applicant for ANESTHESIA MACHINE?

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

What is the FDA product code for ANESTHESIA MACHINE?

The FDA product code for ANESTHESIA MACHINE 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Foregger 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.

K760263I.P.P.B. MANIFOLD/NEBULIZER (CIRCUIT)

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.

K253330A5 Anesthesia System (A5); A7 Anesthesia System (A7)Shenzhen Mindray Bio-Medical Electronics Co., Ltd.K252746Atlan (A100); Atlan (A100 XL); Atlan(A350); Atlan (A350 XL)Drägerwerk AG Co. KgaaK251352Codonics Safe Labeling System-Point of Care Station (PCS) (SLS-700i and related 610i, 620i, 630i series enabled to retrofit RFID features); Codonics Safe Labeling System-Point of Care Station (PCS) (SLS-1, SLS XXX, Multiple Models Pending Configuration)Codonics.IncorporatedK230931AtlanDrägerwerk AG Co. KgaaK213867Carestation 750/750cDatex-Ohmeda, Inc.K201957A8, A9 Anesthesia SystemShenzhen Mindray Bio-Medical Electronics Co., Ltd.

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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