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FDA 510(k)

MAGILL CATHETER INTRO. FORCEPS

K-Number: K801273 · 1980-07-28

ApplicantJ. Sklar Mfg. Co., Inc.
Decision Date1980-07-28
Product CodeKOA
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MAGILL CATHETER INTRO. 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 1980-07-28 under 510(k) number K801273. 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 MAGILL CATHETER INTRO. FORCEPS?

MAGILL CATHETER INTRO. FORCEPS is a medical device that received FDA 510(k) clearance on 1980-07-28. The listed applicant is J. Sklar Mfg. Co., Inc.. The 510(k) number is K801273.

When did MAGILL CATHETER INTRO. FORCEPS receive FDA 510(k) clearance?

MAGILL CATHETER INTRO. FORCEPS received FDA 510(k) clearance on 1980-07-28, under 510(k) number K801273.

Who is the listed applicant for MAGILL CATHETER INTRO. 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 MAGILL CATHETER INTRO. FORCEPS?

The FDA product code for MAGILL CATHETER INTRO. FORCEPS is KOA.

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

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K843693JACOBS HIGH VACUUM SUCTION UNIT 05-2570K842112TISCHLER CERVICAL BIOPSY PUNCH FORCEPSK842111KOGAN ENDOSPECULUM 9-1/2K822448SCISSORS, VARIOUSK802457KEVORKIAN-YOUNGE BIOPSY PUNCH, #90-6610K802458KEVORKIAN-YOUNGE BIOPSY CURETTE #90-6611

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Related Devices (Code: KOA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K182664FiXcisionAgency For Medical Innovations GmbHK950267URETHRAL SUTURE GUIDEApplied Medical ResourcesK932465LI VASECTOMYFemcare , Ltd.K921546VASOVASOSTOMY SETCook Urological, Inc.K931181VESITEC SUTURE PASSERVesitec Medical, Inc.K921304DDV LIGATORNorth American Medical, Inc.

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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