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FDA 510(k)

GRIESHABER SNARE INSTRUMENT AND SNARE CARTRIDGE

K-Number: K914588 · 1992-06-11

ApplicantGrieshaber & Co.
Decision Date1992-06-11
Product CodeGAW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

GRIESHABER SNARE INSTRUMENT AND SNARE CARTRIDGE is the device name listed in this FDA 510(k) record. The listed applicant is Grieshaber & Co.. It received FDA 510(k) clearance on 1992-06-11 under 510(k) number K914588. The device is classified under product code GAW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GRIESHABER SNARE INSTRUMENT AND SNARE CARTRIDGE?

GRIESHABER SNARE INSTRUMENT AND SNARE CARTRIDGE is a medical device that received FDA 510(k) clearance on 1992-06-11. The listed applicant is Grieshaber & Co.. The 510(k) number is K914588.

When did GRIESHABER SNARE INSTRUMENT AND SNARE CARTRIDGE receive FDA 510(k) clearance?

GRIESHABER SNARE INSTRUMENT AND SNARE CARTRIDGE received FDA 510(k) clearance on 1992-06-11, under 510(k) number K914588.

Who is the listed applicant for GRIESHABER SNARE INSTRUMENT AND SNARE CARTRIDGE?

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 GRIESHABER SNARE INSTRUMENT AND SNARE CARTRIDGE?

The FDA product code for GRIESHABER SNARE INSTRUMENT AND SNARE CARTRIDGE is GAW.

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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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