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FDA 510(k)

STER-O-DOSE

K-Number: K820227 · 1982-02-23

ApplicantInhalation Therapy Equipment, Co.
Decision Date1982-02-23
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

STER-O-DOSE is the device name listed in this FDA 510(k) record. The listed applicant is Inhalation Therapy Equipment, Co.. It received FDA 510(k) clearance on 1982-02-23 under 510(k) number K820227. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STER-O-DOSE?

STER-O-DOSE is a medical device that received FDA 510(k) clearance on 1982-02-23. The listed applicant is Inhalation Therapy Equipment, Co.. The 510(k) number is K820227.

When did STER-O-DOSE receive FDA 510(k) clearance?

STER-O-DOSE received FDA 510(k) clearance on 1982-02-23, under 510(k) number K820227.

Who is the listed applicant for STER-O-DOSE?

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

What is the FDA product code for STER-O-DOSE?

The FDA product code for STER-O-DOSE is CAF.

Other records listing Inhalation Therapy 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.

K821191STER-O-MIST 1000 MLK820128UNI-SET

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Official Source

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