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FDA 510(k)

SILICONE OIL 350 CNETISTOKE

K-Number: K854273 · 1985-11-22

ApplicantPacific Medical Industries
Decision Date1985-11-22
Product CodeKRD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SILICONE OIL 350 CNETISTOKE is the device name listed in this FDA 510(k) record. The listed applicant is Pacific Medical Industries. It received FDA 510(k) clearance on 1985-11-22 under 510(k) number K854273. The device is classified under product code KRD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SILICONE OIL 350 CNETISTOKE?

SILICONE OIL 350 CNETISTOKE is a medical device that received FDA 510(k) clearance on 1985-11-22. The listed applicant is Pacific Medical Industries. The 510(k) number is K854273.

When did SILICONE OIL 350 CNETISTOKE receive FDA 510(k) clearance?

SILICONE OIL 350 CNETISTOKE received FDA 510(k) clearance on 1985-11-22, under 510(k) number K854273.

Who is the listed applicant for SILICONE OIL 350 CNETISTOKE?

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

What is the FDA product code for SILICONE OIL 350 CNETISTOKE?

The FDA product code for SILICONE OIL 350 CNETISTOKE is KRD.

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Related Devices (Code: KRD)

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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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