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FDA 510(k)

HSV LAPAROSCOPY SET

K-Number: K941541 · 1994-05-16

ApplicantHenke Sass Wolf of America, Inc.
Decision Date1994-05-16
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

HSV LAPAROSCOPY SET is the device name listed in this FDA 510(k) record. The listed applicant is Henke Sass Wolf of America, Inc.. It received FDA 510(k) clearance on 1994-05-16 under 510(k) number K941541. 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 HSV LAPAROSCOPY SET?

HSV LAPAROSCOPY SET is a medical device that received FDA 510(k) clearance on 1994-05-16. The listed applicant is Henke Sass Wolf of America, Inc.. The 510(k) number is K941541.

When did HSV LAPAROSCOPY SET receive FDA 510(k) clearance?

HSV LAPAROSCOPY SET received FDA 510(k) clearance on 1994-05-16, under 510(k) number K941541.

Who is the listed applicant for HSV LAPAROSCOPY SET?

The FDA 510(k) record lists Henke Sass Wolf of America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HSV LAPAROSCOPY SET?

The FDA product code for HSV LAPAROSCOPY SET is GCJ.

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Other records listing Henke Sass Wolf of America, 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.

K080560HENKE SASS WOLF OF AMERICA ARTHROSCOPEK050163HENKE SASS WOLF OF AMERICA BARIATRIC LAPAROSCOPEK030572HENKE SASS WOLF OF AMERICA NASOPHARYNGOSCOPEK013611HENKE SASS WOLF SAPHENOUS VEIN LAPAROSCOPEK991563CONTINUOUS FLOW HYSTERO-RESECTOSCOPE, KNIFE ELECTRODE, SPIKE ELECTRODE, VAPORISATION ELECTRODE, COAGULATION ELECTRODE, CK983067FINE-JECT

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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.

K262397CuratOR EX2742Eizo CorporationK260884UNIDRIVE Select SystemKarl Storz SE & CO. KGK260972OEV-271MUH LCD Monitor;OEV-321MUH LCD Monitor;OEV-431MUH LCD MonitorSony CorporationK261139VereSee (VER150, VER200, VER151, VER201, VER200C, and VER-100-103)Freyja Healthcare, LLCK253541EZ-Close™ (EZ Close Port Site Closing Device, EZ Close MAX Port Site Closing Device, EZ Close II Port Site Closing Device)Medical ImpactK261614LED LCD Monitor (OEV-271H)Lg Electronics.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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