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FDA 510(k)

ICAN CYLINDRICAL SPONGES

K-Number: K914086 · 1991-10-09

ApplicantIcn Pharmaceuticals, Inc.
Decision Date1991-10-09
Product CodeGDX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ICAN CYLINDRICAL SPONGES is the device name listed in this FDA 510(k) record. The listed applicant is Icn Pharmaceuticals, Inc.. It received FDA 510(k) clearance on 1991-10-09 under 510(k) number K914086. The device is classified under product code GDX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ICAN CYLINDRICAL SPONGES?

ICAN CYLINDRICAL SPONGES is a medical device that received FDA 510(k) clearance on 1991-10-09. The listed applicant is Icn Pharmaceuticals, Inc.. The 510(k) number is K914086.

When did ICAN CYLINDRICAL SPONGES receive FDA 510(k) clearance?

ICAN CYLINDRICAL SPONGES received FDA 510(k) clearance on 1991-10-09, under 510(k) number K914086.

Who is the listed applicant for ICAN CYLINDRICAL SPONGES?

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

What is the FDA product code for ICAN CYLINDRICAL SPONGES?

The FDA product code for ICAN CYLINDRICAL SPONGES is GDX.

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Other records listing Icn Pharmaceuticals, Inc. 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.

K022817COOLTOUCH ND:YAG LASER SYSTEM, MODEL COOLTOUCH, COOLTOUCH-II ND:YAG LASER SYSTEM, MODEL COOLTOUCH-IIK951329IMMUCHEM GAL-MW EAK914530ICAN GT DRAINAGE BAGK914082SUAN FLAT DISSECTOR SPONGESK914083ICAN K DISSECTOR SPONGESK914081ICAN COTTON RAYON BALLS

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Related Devices (Code: GDX)

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.

K923689SURGISTAR BLADESSurgistar, Inc.K921167ULTRABLADEMicron Technology, Inc.K904505CCI CORNEAL SCARIFIERBuckman Co., Inc.K9053801-CUT ACL GRAFT KNIFEDepuy, Inc.K895682VESSEL LOOPSApplied Medical TechnologiesK893033MINI-DIAMOND KNIFEL.A.B. Instruments

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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