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FDA 510(k)

TRI-SERVICE OMV VAPORIZER

K-Number: K864589 · 1987-06-05

ApplicantBear Medical Systems, Inc.
Decision Date1987-06-05
Product CodeBSZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

TRI-SERVICE OMV VAPORIZER is the device name listed in this FDA 510(k) record. The listed applicant is Bear Medical Systems, Inc.. It received FDA 510(k) clearance on 1987-06-05 under 510(k) number K864589. 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 TRI-SERVICE OMV VAPORIZER?

TRI-SERVICE OMV VAPORIZER is a medical device that received FDA 510(k) clearance on 1987-06-05. The listed applicant is Bear Medical Systems, Inc.. The 510(k) number is K864589.

When did TRI-SERVICE OMV VAPORIZER receive FDA 510(k) clearance?

TRI-SERVICE OMV VAPORIZER received FDA 510(k) clearance on 1987-06-05, under 510(k) number K864589.

Who is the listed applicant for TRI-SERVICE OMV VAPORIZER?

The FDA 510(k) record lists Bear Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TRI-SERVICE OMV VAPORIZER?

The FDA product code for TRI-SERVICE OMV VAPORIZER is BSZ.

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Other records listing Bear Medical Systems, 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.

K992788BEAR CUB 750 PSVK983981BEAR 1000, VEOLAR W LEONARDO GRAPHICS, BICORE CP-2000, BICORE CP-100, HI-LO JET ET TUBEK912619BEAR 7 VENTILATORK900637BEAR CEM CONTROLLERK896315BEAR VH820 DISPOSABLE CHAMBER ASSEMBLYK893034VHS 820 HUMIDIFIER, MODIFICATION

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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

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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