FDA 510(k)

SUR-FIT DISPOSABLE CONVEX INSERT

K-Number: K811239 · 1981-06-09

Decision Date1981-06-09

Product CodeEXB

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

SUR-FIT DISPOSABLE CONVEX INSERT is the device name listed in this FDA 510(k) record. The listed applicant is E. R. Squibb & Sons, Inc.. It received FDA 510(k) clearance on 1981-06-09 under 510(k) number K811239. The device is classified under product code EXB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUR-FIT DISPOSABLE CONVEX INSERT?

SUR-FIT DISPOSABLE CONVEX INSERT is a medical device that received FDA 510(k) clearance on 1981-06-09. The listed applicant is E. R. Squibb & Sons, Inc.. The 510(k) number is K811239.

When did SUR-FIT DISPOSABLE CONVEX INSERT receive FDA 510(k) clearance?

SUR-FIT DISPOSABLE CONVEX INSERT received FDA 510(k) clearance on 1981-06-09, under 510(k) number K811239.

Who is the listed applicant for SUR-FIT DISPOSABLE CONVEX INSERT?

The FDA 510(k) record lists E. R. Squibb & Sons, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUR-FIT DISPOSABLE CONVEX INSERT?

The FDA product code for SUR-FIT DISPOSABLE CONVEX INSERT is EXB.

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Other records listing E. R. Squibb & Sons, Inc. as applicant

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Related Devices (Code: EXB)

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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.