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FDA 510(k)

MARLOW/REDDICK LAPAROSCOPIC GRASPING FORCEPS

K-Number: K913964 · 1991-10-23

ApplicantMarlo Surgical Technology
Decision Date1991-10-23
Product CodeHTD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MARLOW/REDDICK LAPAROSCOPIC GRASPING 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 1991-10-23 under 510(k) number K913964. The device is classified under product code HTD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MARLOW/REDDICK LAPAROSCOPIC GRASPING FORCEPS?

MARLOW/REDDICK LAPAROSCOPIC GRASPING FORCEPS is a medical device that received FDA 510(k) clearance on 1991-10-23. The listed applicant is Marlo Surgical Technology. The 510(k) number is K913964.

When did MARLOW/REDDICK LAPAROSCOPIC GRASPING FORCEPS receive FDA 510(k) clearance?

MARLOW/REDDICK LAPAROSCOPIC GRASPING FORCEPS received FDA 510(k) clearance on 1991-10-23, under 510(k) number K913964.

Who is the listed applicant for MARLOW/REDDICK LAPAROSCOPIC GRASPING 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 MARLOW/REDDICK LAPAROSCOPIC GRASPING FORCEPS?

The FDA product code for MARLOW/REDDICK LAPAROSCOPIC GRASPING FORCEPS is HTD.

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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: HTD)

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.

K051281THE NEEDLE CATCHERE.D.Medical , Ltd.K974595CUSHING BAYONET, INSULATED BIPOLAR FORCEPTitan Mfg., Inc.K974594SEMKIN BIPOLAR FORCEPTitan Mfg., Inc.K974593SEMKIN INSULATED BIPOLAR FORCEPTitan Mfg., Inc.K911180CLAW (5MM/10MM) ATRAUMATIC GRASP/MICRO FORCEPSNorthgate Technologies, Inc.K895212TIK EXTRAKTORInstruments of Sweden, 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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