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FDA 510(k)

CLARKE LAPAROSCOPIC LIGATOR AND FORCEPS

K-Number: K903560 · 1990-11-06

ApplicantMarlo Surgical Technology
Decision Date1990-11-06
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CLARKE LAPAROSCOPIC LIGATOR AND FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Marlo Surgical Technology. It received FDA 510(k) clearance on 1990-11-06 under 510(k) number K903560. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLARKE LAPAROSCOPIC LIGATOR AND FORCEPS?

CLARKE LAPAROSCOPIC LIGATOR AND FORCEPS is a medical device that received FDA 510(k) clearance on 1990-11-06. The listed applicant is Marlo Surgical Technology. The 510(k) number is K903560.

When did CLARKE LAPAROSCOPIC LIGATOR AND FORCEPS receive FDA 510(k) clearance?

CLARKE LAPAROSCOPIC LIGATOR AND FORCEPS received FDA 510(k) clearance on 1990-11-06, under 510(k) number K903560.

Who is the listed applicant for CLARKE LAPAROSCOPIC LIGATOR AND FORCEPS?

The FDA 510(k) record lists Marlo Surgical Technology as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CLARKE LAPAROSCOPIC LIGATOR AND FORCEPS?

The FDA product code for CLARKE LAPAROSCOPIC LIGATOR AND FORCEPS is HET.

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Other records listing Marlo Surgical Technology 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.

K960810BALLOON CANNULA 15MM X 35MM,15MM X 55MM, 10/12MM X 55MM,10/12MM X 35MM,5MM X 35MM,2MM X 35MMK962273MALLEABLE STYLET 18 CM ME1816ST, 23 CM ME1816NSTK924611IRRIGATION PUMP AND TUBING SETK932634NU-TIP(TM) FORCEPS:GRASPERS/DISSECTORS/SUTURESK932832PRIMUS INSULATED FORCEPSK920611MARLOW LAPAROSCOPIC GRASPING FORCEP

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Related Devices (Code: HET)

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.

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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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