FDA 510(k)

RUDD-CLINIC HEMORRHOIDAL FORCEPS

K-Number: K800441 · 1980-04-08

Decision Date1980-04-08

Product CodeKOA

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

RUDD-CLINIC HEMORRHOIDAL FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is J. Sklar Mfg. Co., Inc.. It received FDA 510(k) clearance on 1980-04-08 under 510(k) number K800441. The device is classified under product code KOA. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RUDD-CLINIC HEMORRHOIDAL FORCEPS?

RUDD-CLINIC HEMORRHOIDAL FORCEPS is a medical device that received FDA 510(k) clearance on 1980-04-08. The listed applicant is J. Sklar Mfg. Co., Inc.. The 510(k) number is K800441.

When did RUDD-CLINIC HEMORRHOIDAL FORCEPS receive FDA 510(k) clearance?

RUDD-CLINIC HEMORRHOIDAL FORCEPS received FDA 510(k) clearance on 1980-04-08, under 510(k) number K800441.

Who is the listed applicant for RUDD-CLINIC HEMORRHOIDAL FORCEPS?

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

What is the FDA product code for RUDD-CLINIC HEMORRHOIDAL FORCEPS?

The FDA product code for RUDD-CLINIC HEMORRHOIDAL FORCEPS is KOA.

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Other records listing J. Sklar Mfg. Co., Inc. as applicant

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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.