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FDA 510(k)

EMERGIENCY RESUSCITATOR/INHALOR W/ASPIR.

K-Number: K800456 · 1980-03-18

ApplicantKhi, Inc.
Decision Date1980-03-18
Product CodeBTL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

EMERGIENCY RESUSCITATOR/INHALOR W/ASPIR. is the device name listed in this FDA 510(k) record. The listed applicant is Khi, Inc.. It received FDA 510(k) clearance on 1980-03-18 under 510(k) number K800456. The device is classified under product code BTL. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EMERGIENCY RESUSCITATOR/INHALOR W/ASPIR.?

EMERGIENCY RESUSCITATOR/INHALOR W/ASPIR. is a medical device that received FDA 510(k) clearance on 1980-03-18. The listed applicant is Khi, Inc.. The 510(k) number is K800456.

When did EMERGIENCY RESUSCITATOR/INHALOR W/ASPIR. receive FDA 510(k) clearance?

EMERGIENCY RESUSCITATOR/INHALOR W/ASPIR. received FDA 510(k) clearance on 1980-03-18, under 510(k) number K800456.

Who is the listed applicant for EMERGIENCY RESUSCITATOR/INHALOR W/ASPIR.?

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

What is the FDA product code for EMERGIENCY RESUSCITATOR/INHALOR W/ASPIR.?

The FDA product code for EMERGIENCY RESUSCITATOR/INHALOR W/ASPIR. is BTL.

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.

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Other records listing Khi, 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.

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Related Devices (Code: BTL)

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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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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