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FDA 510(k)

STICKIT

K-Number: K935407 · 1994-08-05

Decision Date1994-08-05
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STICKIT is the device name listed in this FDA 510(k) record. The listed applicant is E.M. Innovations, Inc.. It received FDA 510(k) clearance on 1994-08-05 under 510(k) number K935407. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STICKIT?

STICKIT is a medical device that received FDA 510(k) clearance on 1994-08-05. The listed applicant is E.M. Innovations, Inc.. The 510(k) number is K935407.

When did STICKIT receive FDA 510(k) clearance?

STICKIT received FDA 510(k) clearance on 1994-08-05, under 510(k) number K935407.

Who is the listed applicant for STICKIT?

The FDA 510(k) record lists E.M. Innovations, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STICKIT?

The FDA product code for STICKIT is FMI.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: FMI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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