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FDA 510(k)

REGULATOR OXYGEN MECHANICAL

K-Number: K863711 · 1987-01-27

Decision Date1987-01-27
Product CodeCAN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

REGULATOR OXYGEN MECHANICAL is the device name listed in this FDA 510(k) record. The listed applicant is Lifeguard Medical Products, Inc.. It received FDA 510(k) clearance on 1987-01-27 under 510(k) number K863711. The device is classified under product code CAN. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REGULATOR OXYGEN MECHANICAL?

REGULATOR OXYGEN MECHANICAL is a medical device that received FDA 510(k) clearance on 1987-01-27. The listed applicant is Lifeguard Medical Products, Inc.. The 510(k) number is K863711.

When did REGULATOR OXYGEN MECHANICAL receive FDA 510(k) clearance?

REGULATOR OXYGEN MECHANICAL received FDA 510(k) clearance on 1987-01-27, under 510(k) number K863711.

Who is the listed applicant for REGULATOR OXYGEN MECHANICAL?

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

What is the FDA product code for REGULATOR OXYGEN MECHANICAL?

The FDA product code for REGULATOR OXYGEN MECHANICAL is CAN.

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 Lifeguard Medical Products, 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.

View all 12 devices →

Related Devices (Code: CAN)

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

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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