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FDA 510(k)

JEHLE CORONARY PERFUSION CATHETERS

K-Number: K874242 · 1987-12-07

ApplicantPilling Co.
Decision Date1987-12-07
Product CodeKRA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

JEHLE CORONARY PERFUSION CATHETERS is the device name listed in this FDA 510(k) record. The listed applicant is Pilling Co.. It received FDA 510(k) clearance on 1987-12-07 under 510(k) number K874242. The device is classified under product code KRA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JEHLE CORONARY PERFUSION CATHETERS?

JEHLE CORONARY PERFUSION CATHETERS is a medical device that received FDA 510(k) clearance on 1987-12-07. The listed applicant is Pilling Co.. The 510(k) number is K874242.

When did JEHLE CORONARY PERFUSION CATHETERS receive FDA 510(k) clearance?

JEHLE CORONARY PERFUSION CATHETERS received FDA 510(k) clearance on 1987-12-07, under 510(k) number K874242.

Who is the listed applicant for JEHLE CORONARY PERFUSION CATHETERS?

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

What is the FDA product code for JEHLE CORONARY PERFUSION CATHETERS?

The FDA product code for JEHLE CORONARY PERFUSION CATHETERS is KRA.

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Other records listing Pilling Co. 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.

K934427PILLING LAPAROSCOPIC INSTRUMENTATIONK925370TRIANGULAR JAW MICROLARYNGEAL FORCEPSK925198KAISER NO CANNULA THORACOSCOPY/LAPAROSCOPY INSTRK922971NO-SCALPEL VASCETOMY INSTRUMENTSK914015CLEMENT-PILLING CHOLANGIOGRAPHY CATH GUIDE/CLAMPK911099MEHIGAN-PILLING ANGIOSCOPIC VASCULAR INSTRUM. LINE

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Related Devices (Code: KRA)

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.

K253509TriSalus TriNav Advance Infusion SystemTrisalus Life SciencesK254051Extroducer Infusion Catheter SystemSmartWise Sweden ABK261610Verge™ MicrocatheterInstylla, Inc.K260771TruSelect™ 2.6 MicrocatheterBoston Scientific CorporationK250794InVera Infusion DeviceInvera MedicalK243534Micro CatheterSuzhou Zenith Vascular SciTech Limited

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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