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FDA 510(k)

TUBAL LUMEN SUPPORT

K-Number: K932114 · 1994-09-27

ApplicantCook Ob/Gyn
Decision Date1994-09-27
Product CodeHFJ
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

TUBAL LUMEN SUPPORT is the device name listed in this FDA 510(k) record. The listed applicant is Cook Ob/Gyn. It received FDA 510(k) clearance on 1994-09-27 under 510(k) number K932114. The device is classified under product code HFJ. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TUBAL LUMEN SUPPORT?

TUBAL LUMEN SUPPORT is a medical device that received FDA 510(k) clearance on 1994-09-27. The listed applicant is Cook Ob/Gyn. The 510(k) number is K932114.

When did TUBAL LUMEN SUPPORT receive FDA 510(k) clearance?

TUBAL LUMEN SUPPORT received FDA 510(k) clearance on 1994-09-27, under 510(k) number K932114.

Who is the listed applicant for TUBAL LUMEN SUPPORT?

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

What is the FDA product code for TUBAL LUMEN SUPPORT?

The FDA product code for TUBAL LUMEN SUPPORT is HFJ.

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Other records listing Cook Ob/Gyn 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.

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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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