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FDA 510(k)

MK 808 SERIES NASAL OXYGEN SAMPLER

K-Number: K822608 · 1982-10-04

Decision Date1982-10-04
Product CodeCCL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MK 808 SERIES NASAL OXYGEN SAMPLER 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 1982-10-04 under 510(k) number K822608. The device is classified under product code CCL. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MK 808 SERIES NASAL OXYGEN SAMPLER?

MK 808 SERIES NASAL OXYGEN SAMPLER is a medical device that received FDA 510(k) clearance on 1982-10-04. The listed applicant is Instrumentation Industries, Inc.. The 510(k) number is K822608.

When did MK 808 SERIES NASAL OXYGEN SAMPLER receive FDA 510(k) clearance?

MK 808 SERIES NASAL OXYGEN SAMPLER received FDA 510(k) clearance on 1982-10-04, under 510(k) number K822608.

Who is the listed applicant for MK 808 SERIES NASAL OXYGEN SAMPLER?

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 MK 808 SERIES NASAL OXYGEN SAMPLER?

The FDA product code for MK 808 SERIES NASAL OXYGEN SAMPLER is CCL.

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: CCL)

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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