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FDA 510(k)

PORT-A-BOUT 240

K-Number: K772216 · 1978-01-05

ApplicantHudson Oxygen Therapy Sales Co.
Decision Date1978-01-05
Product CodeCAN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PORT-A-BOUT 240 is the device name listed in this FDA 510(k) record. The listed applicant is Hudson Oxygen Therapy Sales Co.. It received FDA 510(k) clearance on 1978-01-05 under 510(k) number K772216. 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 PORT-A-BOUT 240?

PORT-A-BOUT 240 is a medical device that received FDA 510(k) clearance on 1978-01-05. The listed applicant is Hudson Oxygen Therapy Sales Co.. The 510(k) number is K772216.

When did PORT-A-BOUT 240 receive FDA 510(k) clearance?

PORT-A-BOUT 240 received FDA 510(k) clearance on 1978-01-05, under 510(k) number K772216.

Who is the listed applicant for PORT-A-BOUT 240?

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

What is the FDA product code for PORT-A-BOUT 240?

The FDA product code for PORT-A-BOUT 240 is CAN.

Other records listing Hudson Oxygen Therapy Sales 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.

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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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