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FDA 510(k)

ANESTHESIA APPARATUS #FO 20S

K-Number: K830160 · 1983-03-09

ApplicantW.E. Leder Enterprises, Inc.
Decision Date1983-03-09
Product CodeBSZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ANESTHESIA APPARATUS #FO 20S is the device name listed in this FDA 510(k) record. The listed applicant is W.E. Leder Enterprises, Inc.. It received FDA 510(k) clearance on 1983-03-09 under 510(k) number K830160. 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 APPARATUS #FO 20S?

ANESTHESIA APPARATUS #FO 20S is a medical device that received FDA 510(k) clearance on 1983-03-09. The listed applicant is W.E. Leder Enterprises, Inc.. The 510(k) number is K830160.

When did ANESTHESIA APPARATUS #FO 20S receive FDA 510(k) clearance?

ANESTHESIA APPARATUS #FO 20S received FDA 510(k) clearance on 1983-03-09, under 510(k) number K830160.

Who is the listed applicant for ANESTHESIA APPARATUS #FO 20S?

The FDA 510(k) record lists W.E. Leder Enterprises, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ANESTHESIA APPARATUS #FO 20S?

The FDA product code for ANESTHESIA APPARATUS #FO 20S 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.

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Other records listing W.E. Leder Enterprises, 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.

K831877ARF 850 EK831981LARYNGESCOPEK831878CARDIO-SCOPE MINI MONITORK830161ANESTHESIA APATATUS #D-25K830159ANESTHESIA APPARATUS PH-35

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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