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FDA 510(k)

MODEL 5460 + 5480 POP-OFF VALVES

K-Number: K802591 · 1980-11-12

ApplicantG. Dundas Co.
Decision Date1980-11-12
Product CodeBSZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MODEL 5460 + 5480 POP-OFF VALVES is the device name listed in this FDA 510(k) record. The listed applicant is G. Dundas Co.. It received FDA 510(k) clearance on 1980-11-12 under 510(k) number K802591. 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 MODEL 5460 + 5480 POP-OFF VALVES?

MODEL 5460 + 5480 POP-OFF VALVES is a medical device that received FDA 510(k) clearance on 1980-11-12. The listed applicant is G. Dundas Co.. The 510(k) number is K802591.

When did MODEL 5460 + 5480 POP-OFF VALVES receive FDA 510(k) clearance?

MODEL 5460 + 5480 POP-OFF VALVES received FDA 510(k) clearance on 1980-11-12, under 510(k) number K802591.

Who is the listed applicant for MODEL 5460 + 5480 POP-OFF VALVES?

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

What is the FDA product code for MODEL 5460 + 5480 POP-OFF VALVES?

The FDA product code for MODEL 5460 + 5480 POP-OFF VALVES 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 G. Dundas Co. 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.

K963601MODEL 1920 WASTE GAS SCAVENGER

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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