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FDA 510(k)

SI-PRO

K-Number: K904389 · 1990-12-17

ApplicantDavid F. Trungale
Decision Date1990-12-17
Product CodeEYF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SI-PRO is the device name listed in this FDA 510(k) record. The listed applicant is David F. Trungale. It received FDA 510(k) clearance on 1990-12-17 under 510(k) number K904389. The device is classified under product code EYF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SI-PRO?

SI-PRO is a medical device that received FDA 510(k) clearance on 1990-12-17. The listed applicant is David F. Trungale. The 510(k) number is K904389.

When did SI-PRO receive FDA 510(k) clearance?

SI-PRO received FDA 510(k) clearance on 1990-12-17, under 510(k) number K904389.

Who is the listed applicant for SI-PRO?

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

What is the FDA product code for SI-PRO?

The FDA product code for SI-PRO is EYF.

Related Devices (Code: EYF)

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.

K922785IRRIVAGEAutovageK911407HARDING STERNAL SHIELDHarding Medical DevicesK910104ANTI-FOG DISPOSABLE IV INDUCTION COVERCentral Plastic, Inc.K832908COMFEEL PROTECTIVE RINGSColoplast A/S

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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