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FDA 510(k)

NU-TIP(TM) FORCEPS:GRASPERS/DISSECTORS/SUTURES

K-Number: K932634 · 1994-02-25

ApplicantMarlo Surgical Technology
Decision Date1994-02-25
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

NU-TIP(TM) FORCEPS:GRASPERS/DISSECTORS/SUTURES 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 1994-02-25 under 510(k) number K932634. 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 NU-TIP(TM) FORCEPS:GRASPERS/DISSECTORS/SUTURES?

NU-TIP(TM) FORCEPS:GRASPERS/DISSECTORS/SUTURES is a medical device that received FDA 510(k) clearance on 1994-02-25. The listed applicant is Marlo Surgical Technology. The 510(k) number is K932634.

When did NU-TIP(TM) FORCEPS:GRASPERS/DISSECTORS/SUTURES receive FDA 510(k) clearance?

NU-TIP(TM) FORCEPS:GRASPERS/DISSECTORS/SUTURES received FDA 510(k) clearance on 1994-02-25, under 510(k) number K932634.

Who is the listed applicant for NU-TIP(TM) FORCEPS:GRASPERS/DISSECTORS/SUTURES?

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 NU-TIP(TM) FORCEPS:GRASPERS/DISSECTORS/SUTURES?

The FDA product code for NU-TIP(TM) FORCEPS:GRASPERS/DISSECTORS/SUTURES 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 SETK932832PRIMUS INSULATED FORCEPSK920611MARLOW LAPAROSCOPIC GRASPING FORCEPK914153OTT INSUFFLATOR FILTER PLUS/TUBING SET

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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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