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FDA 510(k)

ASPIRATOR, MANUEL

K-Number: K780208 · 1978-03-03

ApplicantDade, Baxter Travenol Diagnostics, Inc.
Decision Date1978-03-03
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ASPIRATOR, MANUEL is the device name listed in this FDA 510(k) record. The listed applicant is Dade, Baxter Travenol Diagnostics, Inc.. It received FDA 510(k) clearance on 1978-03-03 under 510(k) number K780208. The device is classified under product code JQW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASPIRATOR, MANUEL?

ASPIRATOR, MANUEL is a medical device that received FDA 510(k) clearance on 1978-03-03. The listed applicant is Dade, Baxter Travenol Diagnostics, Inc.. The 510(k) number is K780208.

When did ASPIRATOR, MANUEL receive FDA 510(k) clearance?

ASPIRATOR, MANUEL received FDA 510(k) clearance on 1978-03-03, under 510(k) number K780208.

Who is the listed applicant for ASPIRATOR, MANUEL?

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

What is the FDA product code for ASPIRATOR, MANUEL?

The FDA product code for ASPIRATOR, MANUEL is JQW.

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Related Devices (Code: JQW)

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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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