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FDA 510(k)

MS-303-OXYGEN REGULATOR SHIELD

K-Number: K810679 · 1981-04-17

Decision Date1981-04-17
Product CodeCAN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MS-303-OXYGEN REGULATOR SHIELD is the device name listed in this FDA 510(k) record. The listed applicant is Instrumentation Industries, Inc.. It received FDA 510(k) clearance on 1981-04-17 under 510(k) number K810679. 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 MS-303-OXYGEN REGULATOR SHIELD?

MS-303-OXYGEN REGULATOR SHIELD is a medical device that received FDA 510(k) clearance on 1981-04-17. The listed applicant is Instrumentation Industries, Inc.. The 510(k) number is K810679.

When did MS-303-OXYGEN REGULATOR SHIELD receive FDA 510(k) clearance?

MS-303-OXYGEN REGULATOR SHIELD received FDA 510(k) clearance on 1981-04-17, under 510(k) number K810679.

Who is the listed applicant for MS-303-OXYGEN REGULATOR SHIELD?

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

What is the FDA product code for MS-303-OXYGEN REGULATOR SHIELD?

The FDA product code for MS-303-OXYGEN REGULATOR SHIELD 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 Instrumentation Industries, 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 45 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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