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FDA 510(k)

1-125 ENDOSEED

K-Number: K914825 · 1992-03-19

ApplicantEndo Technic Corp.
Decision Date1992-03-19
Product CodeKXK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

1-125 ENDOSEED is the device name listed in this FDA 510(k) record. The listed applicant is Endo Technic Corp.. It received FDA 510(k) clearance on 1992-03-19 under 510(k) number K914825. The device is classified under product code KXK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 1-125 ENDOSEED?

1-125 ENDOSEED is a medical device that received FDA 510(k) clearance on 1992-03-19. The listed applicant is Endo Technic Corp.. The 510(k) number is K914825.

When did 1-125 ENDOSEED receive FDA 510(k) clearance?

1-125 ENDOSEED received FDA 510(k) clearance on 1992-03-19, under 510(k) number K914825.

Who is the listed applicant for 1-125 ENDOSEED?

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

What is the FDA product code for 1-125 ENDOSEED?

The FDA product code for 1-125 ENDOSEED is KXK.

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Other records listing Endo Technic Corp. 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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