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FDA 510(k)

MEGASON MODEL 150

K-Number: K843221 · 1984-08-24

ApplicantBirtcher Corp.
Decision Date1984-08-24
Product CodeIMI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MEGASON MODEL 150 is the device name listed in this FDA 510(k) record. The listed applicant is Birtcher Corp.. It received FDA 510(k) clearance on 1984-08-24 under 510(k) number K843221. The device is classified under product code IMI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEGASON MODEL 150?

MEGASON MODEL 150 is a medical device that received FDA 510(k) clearance on 1984-08-24. The listed applicant is Birtcher Corp.. The 510(k) number is K843221.

When did MEGASON MODEL 150 receive FDA 510(k) clearance?

MEGASON MODEL 150 received FDA 510(k) clearance on 1984-08-24, under 510(k) number K843221.

Who is the listed applicant for MEGASON MODEL 150?

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

What is the FDA product code for MEGASON MODEL 150?

The FDA product code for MEGASON MODEL 150 is IMI.

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Other records listing Birtcher Corp. as applicant

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Related Devices (Code: IMI)

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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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