IFSA STERILE BRAIDED POLY NONABSOR SURG SUTURES
K-Number: K905285 · 1991-02-11
Advertisement
Device Summary
Frequently Asked Questions
What is the IFSA STERILE BRAIDED POLY NONABSOR SURG SUTURES?
IFSA STERILE BRAIDED POLY NONABSOR SURG SUTURES is a medical device that received FDA 510(k) clearance on 1991-02-11. The listed applicant is Internacional Farmaceutica, S.A. DE C.V.. The 510(k) number is K905285.
When did IFSA STERILE BRAIDED POLY NONABSOR SURG SUTURES receive FDA 510(k) clearance?
IFSA STERILE BRAIDED POLY NONABSOR SURG SUTURES received FDA 510(k) clearance on 1991-02-11, under 510(k) number K905285.
Who is the listed applicant for IFSA STERILE BRAIDED POLY NONABSOR SURG SUTURES?
The FDA 510(k) record lists Internacional Farmaceutica, S.A. DE C.V. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IFSA STERILE BRAIDED POLY NONABSOR SURG SUTURES?
The FDA product code for IFSA STERILE BRAIDED POLY NONABSOR SURG SUTURES is GAS.
Related Clinical Trials
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.
Other records listing Internacional Farmaceutica, S.A. DE C.V. 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.
Related Devices (Code: GAS)
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.
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.
Advertisement