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FDA 510(k)

CANNULA, PERFUSION, FALLOPIAN TUBE

K-Number: K772230 · 1978-01-03

ApplicantJ. Sklar Mfg. Co., Inc.
Decision Date1978-01-03
Product CodeLKF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CANNULA, PERFUSION, FALLOPIAN TUBE 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 1978-01-03 under 510(k) number K772230. The device is classified under product code LKF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CANNULA, PERFUSION, FALLOPIAN TUBE?

CANNULA, PERFUSION, FALLOPIAN TUBE is a medical device that received FDA 510(k) clearance on 1978-01-03. The listed applicant is J. Sklar Mfg. Co., Inc.. The 510(k) number is K772230.

When did CANNULA, PERFUSION, FALLOPIAN TUBE receive FDA 510(k) clearance?

CANNULA, PERFUSION, FALLOPIAN TUBE received FDA 510(k) clearance on 1978-01-03, under 510(k) number K772230.

Who is the listed applicant for CANNULA, PERFUSION, FALLOPIAN TUBE?

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 CANNULA, PERFUSION, FALLOPIAN TUBE?

The FDA product code for CANNULA, PERFUSION, FALLOPIAN TUBE is LKF.

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Related Devices (Code: LKF)

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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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