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FDA 510(k)

TERRA FEMME

K-Number: K930400 · 1994-03-14

ApplicantBio Business Intl, Inc.
Decision Date1994-03-14
Product CodeHEB
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

TERRA FEMME is the device name listed in this FDA 510(k) record. The listed applicant is Bio Business Intl, Inc.. It received FDA 510(k) clearance on 1994-03-14 under 510(k) number K930400. The device is classified under product code HEB. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TERRA FEMME?

TERRA FEMME is a medical device that received FDA 510(k) clearance on 1994-03-14. The listed applicant is Bio Business Intl, Inc.. The 510(k) number is K930400.

When did TERRA FEMME receive FDA 510(k) clearance?

TERRA FEMME received FDA 510(k) clearance on 1994-03-14, under 510(k) number K930400.

Who is the listed applicant for TERRA FEMME?

The FDA 510(k) record lists Bio Business Intl, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TERRA FEMME?

The FDA product code for TERRA FEMME is HEB.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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