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FDA 510(k)

INVIRO SYRINGE

K-Number: K941450 · 1994-12-12

ApplicantDr. F. Ross Sharp , Ltd.
Decision Date1994-12-12
Product CodeMEG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INVIRO SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Dr. F. Ross Sharp , Ltd.. It received FDA 510(k) clearance on 1994-12-12 under 510(k) number K941450. The device is classified under product code MEG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INVIRO SYRINGE?

INVIRO SYRINGE is a medical device that received FDA 510(k) clearance on 1994-12-12. The listed applicant is Dr. F. Ross Sharp , Ltd.. The 510(k) number is K941450.

When did INVIRO SYRINGE receive FDA 510(k) clearance?

INVIRO SYRINGE received FDA 510(k) clearance on 1994-12-12, under 510(k) number K941450.

Who is the listed applicant for INVIRO SYRINGE?

The FDA 510(k) record lists Dr. F. Ross Sharp , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INVIRO SYRINGE?

The FDA product code for INVIRO SYRINGE is MEG.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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