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FDA 510(k)

INHALATOR MODELS 8100, 10100 AND 10200

K-Number: K862194 · 1986-07-28

Decision Date1986-07-28
Product CodeCAW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

INHALATOR MODELS 8100, 10100 AND 10200 is the device name listed in this FDA 510(k) record. The listed applicant is U.O. Equipment Co.. It received FDA 510(k) clearance on 1986-07-28 under 510(k) number K862194. The device is classified under product code CAW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INHALATOR MODELS 8100, 10100 AND 10200?

INHALATOR MODELS 8100, 10100 AND 10200 is a medical device that received FDA 510(k) clearance on 1986-07-28. The listed applicant is U.O. Equipment Co.. The 510(k) number is K862194.

When did INHALATOR MODELS 8100, 10100 AND 10200 receive FDA 510(k) clearance?

INHALATOR MODELS 8100, 10100 AND 10200 received FDA 510(k) clearance on 1986-07-28, under 510(k) number K862194.

Who is the listed applicant for INHALATOR MODELS 8100, 10100 AND 10200?

The FDA 510(k) record lists U.O. Equipment Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INHALATOR MODELS 8100, 10100 AND 10200?

The FDA product code for INHALATOR MODELS 8100, 10100 AND 10200 is CAW.

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 U.O. Equipment 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.

Related Devices (Code: CAW)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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