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FDA 510(k)

FEMORAL ANGIOGRAPHY DRAPE

K-Number: K890101 · 1989-03-16

ApplicantMedical Plastics, Inc.
Decision Date1989-03-16
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FEMORAL ANGIOGRAPHY DRAPE is the device name listed in this FDA 510(k) record. The listed applicant is Medical Plastics, Inc.. It received FDA 510(k) clearance on 1989-03-16 under 510(k) number K890101. 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 FEMORAL ANGIOGRAPHY DRAPE?

FEMORAL ANGIOGRAPHY DRAPE is a medical device that received FDA 510(k) clearance on 1989-03-16. The listed applicant is Medical Plastics, Inc.. The 510(k) number is K890101.

When did FEMORAL ANGIOGRAPHY DRAPE receive FDA 510(k) clearance?

FEMORAL ANGIOGRAPHY DRAPE received FDA 510(k) clearance on 1989-03-16, under 510(k) number K890101.

Who is the listed applicant for FEMORAL ANGIOGRAPHY DRAPE?

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

What is the FDA product code for FEMORAL ANGIOGRAPHY DRAPE?

The FDA product code for FEMORAL ANGIOGRAPHY DRAPE is KKX.

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Other records listing Medical Plastics, 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.

K902384ABDOMINAL OR C-SECTION DRAPE SHEETK896088FEMORAL ANGIOGRAPHY DRAPEK895404UNDER BUTTOCKS DRAPEK822072MPI ELECTROSURGICAL CAPACTIVE DISPERK821169MPI MON-IT II, SMART SAFETY SYSTEMK781148ELECTROSURGICAL PENCIL SYSTEM

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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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