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FDA 510(k)

ANESTHESIOLOGY DEVICE

K-Number: K811430 · 1981-06-09

ApplicantVital Air Oxygen Co.
Decision Date1981-06-09
Product CodeCAN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ANESTHESIOLOGY DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Vital Air Oxygen Co.. It received FDA 510(k) clearance on 1981-06-09 under 510(k) number K811430. 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 ANESTHESIOLOGY DEVICE?

ANESTHESIOLOGY DEVICE is a medical device that received FDA 510(k) clearance on 1981-06-09. The listed applicant is Vital Air Oxygen Co.. The 510(k) number is K811430.

When did ANESTHESIOLOGY DEVICE receive FDA 510(k) clearance?

ANESTHESIOLOGY DEVICE received FDA 510(k) clearance on 1981-06-09, under 510(k) number K811430.

Who is the listed applicant for ANESTHESIOLOGY DEVICE?

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

What is the FDA product code for ANESTHESIOLOGY DEVICE?

The FDA product code for ANESTHESIOLOGY DEVICE is CAN.

Related Clinical Trials

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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.

K162811MR Conditional CGA 870Essex Industries, Inc.K080243PORTABLE OXYGEN UNIT SCA900San Cheong Co. , Ltd.K060265REMCORE REMOTE CONTROLLED OXYGEN REGULATORRemcore, Inc.K061785CYL-FIL OXYGEN SYSTEMResponsive Respiratory, Inc.K950777OXYGEN REGULATORMada Medical Products, Inc.K942751VANGUARD SERIES GAS REGULATORSBuckman Co., Inc.

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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