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FDA 510(k)

BARRIER IMPERVIOUS S-OCKINETTE

K-Number: K760890 · 1976-11-11

ApplicantSurgikos, Inc.
Decision Date1976-11-11
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BARRIER IMPERVIOUS S-OCKINETTE is the device name listed in this FDA 510(k) record. The listed applicant is Surgikos, Inc.. It received FDA 510(k) clearance on 1976-11-11 under 510(k) number K760890. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARRIER IMPERVIOUS S-OCKINETTE?

BARRIER IMPERVIOUS S-OCKINETTE is a medical device that received FDA 510(k) clearance on 1976-11-11. The listed applicant is Surgikos, Inc.. The 510(k) number is K760890.

When did BARRIER IMPERVIOUS S-OCKINETTE receive FDA 510(k) clearance?

BARRIER IMPERVIOUS S-OCKINETTE received FDA 510(k) clearance on 1976-11-11, under 510(k) number K760890.

Who is the listed applicant for BARRIER IMPERVIOUS S-OCKINETTE?

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

What is the FDA product code for BARRIER IMPERVIOUS S-OCKINETTE?

The FDA product code for BARRIER IMPERVIOUS S-OCKINETTE is KKX.

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Other records listing Surgikos, Inc. as applicant

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Related Devices (Code: KKX)

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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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