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FDA 510(k)

MARLOW LAPAROSCOPIC SCISSORS

K-Number: K914869 · 1992-01-15

ApplicantMarlo Surgical Technology
Decision Date1992-01-15
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MARLOW LAPAROSCOPIC SCISSORS 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 1992-01-15 under 510(k) number K914869. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MARLOW LAPAROSCOPIC SCISSORS?

MARLOW LAPAROSCOPIC SCISSORS is a medical device that received FDA 510(k) clearance on 1992-01-15. The listed applicant is Marlo Surgical Technology. The 510(k) number is K914869.

When did MARLOW LAPAROSCOPIC SCISSORS receive FDA 510(k) clearance?

MARLOW LAPAROSCOPIC SCISSORS received FDA 510(k) clearance on 1992-01-15, under 510(k) number K914869.

Who is the listed applicant for MARLOW LAPAROSCOPIC SCISSORS?

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 MARLOW LAPAROSCOPIC SCISSORS?

The FDA product code for MARLOW LAPAROSCOPIC SCISSORS is GCJ.

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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 SETK932832PRIMUS INSULATED FORCEPSK932634NU-TIP(TM) FORCEPS:GRASPERS/DISSECTORS/SUTURESK920611MARLOW LAPAROSCOPIC GRASPING FORCEP

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Related Devices (Code: GCJ)

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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