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FDA 510(k)

ORIGIN BALLOON ANCHOR

K-Number: K944304 · 1994-09-23

ApplicantOrigin Medsystems, Inc.
Decision Date1994-09-23
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ORIGIN BALLOON ANCHOR is the device name listed in this FDA 510(k) record. The listed applicant is Origin Medsystems, Inc.. It received FDA 510(k) clearance on 1994-09-23 under 510(k) number K944304. 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 ORIGIN BALLOON ANCHOR?

ORIGIN BALLOON ANCHOR is a medical device that received FDA 510(k) clearance on 1994-09-23. The listed applicant is Origin Medsystems, Inc.. The 510(k) number is K944304.

When did ORIGIN BALLOON ANCHOR receive FDA 510(k) clearance?

ORIGIN BALLOON ANCHOR received FDA 510(k) clearance on 1994-09-23, under 510(k) number K944304.

Who is the listed applicant for ORIGIN BALLOON ANCHOR?

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

What is the FDA product code for ORIGIN BALLOON ANCHOR?

The FDA product code for ORIGIN BALLOON ANCHOR is GCJ.

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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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