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FDA 510(k)

CITATION MEDICAL SCOPE PROCEDURE PACK

K-Number: K912490 · 1991-08-16

ApplicantCitation Medical Corp.
Decision Date1991-08-16
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CITATION MEDICAL SCOPE PROCEDURE PACK is the device name listed in this FDA 510(k) record. The listed applicant is Citation Medical Corp.. It received FDA 510(k) clearance on 1991-08-16 under 510(k) number K912490. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CITATION MEDICAL SCOPE PROCEDURE PACK?

CITATION MEDICAL SCOPE PROCEDURE PACK is a medical device that received FDA 510(k) clearance on 1991-08-16. The listed applicant is Citation Medical Corp.. The 510(k) number is K912490.

When did CITATION MEDICAL SCOPE PROCEDURE PACK receive FDA 510(k) clearance?

CITATION MEDICAL SCOPE PROCEDURE PACK received FDA 510(k) clearance on 1991-08-16, under 510(k) number K912490.

Who is the listed applicant for CITATION MEDICAL SCOPE PROCEDURE PACK?

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

What is the FDA product code for CITATION MEDICAL SCOPE PROCEDURE PACK?

The FDA product code for CITATION MEDICAL SCOPE PROCEDURE PACK is KKX.

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Other records listing Citation Medical 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.

K951941CITATION MULTIPLE USE DELTA SCOPEK945390CITATION DELTA SCOPEK946290CITATION POWER TOOLK951249CITATION SINUSCOPEK944976BRONCHOSCOPE,NON-RIGIDK940847ENDOSCOPIC PLANTAR FASCIA KIT

View all 12 devices →

Related Devices (Code: KKX)

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.

K230645BeneHold™ Surgical Incise Drape with CHG antimicrobial IIAvery Dennison Medical , Ltd.K2225783M™ Ioban™ CHG Chlorhexidine Gluconate Incise Drape (contains 2% w/w CHG)3M CompanyK202208BeneHold Surgical Incise Drape with CHG antimicrobialAvery Dennison Belgie BvbaK200238ControlRad Sterile CoverControlrad, Inc.K163556MediClear PreOpCovalontechnologies, Inc.K130404TIBURON SURGICAL DRAPECardinal Health200, LLC

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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