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FDA 510(k)

G.A.S./GRIESHABER AIR SYSTEM

K-Number: K860502 · 1986-02-27

ApplicantGrieshaber & Co.
Decision Date1986-02-27
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

G.A.S./GRIESHABER AIR SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Grieshaber & Co.. It received FDA 510(k) clearance on 1986-02-27 under 510(k) number K860502. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the G.A.S./GRIESHABER AIR SYSTEM?

G.A.S./GRIESHABER AIR SYSTEM is a medical device that received FDA 510(k) clearance on 1986-02-27. The listed applicant is Grieshaber & Co.. The 510(k) number is K860502.

When did G.A.S./GRIESHABER AIR SYSTEM receive FDA 510(k) clearance?

G.A.S./GRIESHABER AIR SYSTEM received FDA 510(k) clearance on 1986-02-27, under 510(k) number K860502.

Who is the listed applicant for G.A.S./GRIESHABER AIR SYSTEM?

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

What is the FDA product code for G.A.S./GRIESHABER AIR SYSTEM?

The FDA product code for G.A.S./GRIESHABER AIR SYSTEM is FRN.

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Other records listing Grieshaber & Co. as applicant

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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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