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FDA 510(k)

SIEMENS-ELECTROGERATE GMBH MICRO-INHALER

K-Number: K800830 · 1980-06-30

ApplicantMacbeth Sales Corp.
Decision Date1980-06-30
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SIEMENS-ELECTROGERATE GMBH MICRO-INHALER is the device name listed in this FDA 510(k) record. The listed applicant is Macbeth Sales Corp.. It received FDA 510(k) clearance on 1980-06-30 under 510(k) number K800830. 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 SIEMENS-ELECTROGERATE GMBH MICRO-INHALER?

SIEMENS-ELECTROGERATE GMBH MICRO-INHALER is a medical device that received FDA 510(k) clearance on 1980-06-30. The listed applicant is Macbeth Sales Corp.. The 510(k) number is K800830.

When did SIEMENS-ELECTROGERATE GMBH MICRO-INHALER receive FDA 510(k) clearance?

SIEMENS-ELECTROGERATE GMBH MICRO-INHALER received FDA 510(k) clearance on 1980-06-30, under 510(k) number K800830.

Who is the listed applicant for SIEMENS-ELECTROGERATE GMBH MICRO-INHALER?

The FDA 510(k) record lists Macbeth Sales Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SIEMENS-ELECTROGERATE GMBH MICRO-INHALER?

The FDA product code for SIEMENS-ELECTROGERATE GMBH MICRO-INHALER is CAF.

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Official Source

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