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FDA 510(k)

7-510-25 HYSTEROMED TUBING KIT

K-Number: K931606 · 1994-01-24

ApplicantNortech
Decision Date1994-01-24
Product CodeHIG
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

7-510-25 HYSTEROMED TUBING KIT is the device name listed in this FDA 510(k) record. The listed applicant is Nortech. It received FDA 510(k) clearance on 1994-01-24 under 510(k) number K931606. The device is classified under product code HIG. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 7-510-25 HYSTEROMED TUBING KIT?

7-510-25 HYSTEROMED TUBING KIT is a medical device that received FDA 510(k) clearance on 1994-01-24. The listed applicant is Nortech. The 510(k) number is K931606.

When did 7-510-25 HYSTEROMED TUBING KIT receive FDA 510(k) clearance?

7-510-25 HYSTEROMED TUBING KIT received FDA 510(k) clearance on 1994-01-24, under 510(k) number K931606.

Who is the listed applicant for 7-510-25 HYSTEROMED TUBING KIT?

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

What is the FDA product code for 7-510-25 HYSTEROMED TUBING KIT?

The FDA product code for 7-510-25 HYSTEROMED TUBING KIT is HIG.

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Related Devices (Code: HIG)

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

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