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FDA 510(k)

SOPHYCAMERA DSM 315

K-Number: K903030 · 1990-10-29

ApplicantProvino
Decision Date1990-10-29
Product CodeIYX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SOPHYCAMERA DSM 315 is the device name listed in this FDA 510(k) record. The listed applicant is Provino. It received FDA 510(k) clearance on 1990-10-29 under 510(k) number K903030. The device is classified under product code IYX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOPHYCAMERA DSM 315?

SOPHYCAMERA DSM 315 is a medical device that received FDA 510(k) clearance on 1990-10-29. The listed applicant is Provino. The 510(k) number is K903030.

When did SOPHYCAMERA DSM 315 receive FDA 510(k) clearance?

SOPHYCAMERA DSM 315 received FDA 510(k) clearance on 1990-10-29, under 510(k) number K903030.

Who is the listed applicant for SOPHYCAMERA DSM 315?

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

What is the FDA product code for SOPHYCAMERA DSM 315?

The FDA product code for SOPHYCAMERA DSM 315 is IYX.

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Related Devices (Code: IYX)

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.

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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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