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FDA 510(k)

CLEMENT-PILLING CHOLANGIOGRAPHY CATH GUIDE/CLAMP

K-Number: K914015 · 1991-11-21

ApplicantPilling Co.
Decision Date1991-11-21
Product CodeGBZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CLEMENT-PILLING CHOLANGIOGRAPHY CATH GUIDE/CLAMP is the device name listed in this FDA 510(k) record. The listed applicant is Pilling Co.. It received FDA 510(k) clearance on 1991-11-21 under 510(k) number K914015. The device is classified under product code GBZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLEMENT-PILLING CHOLANGIOGRAPHY CATH GUIDE/CLAMP?

CLEMENT-PILLING CHOLANGIOGRAPHY CATH GUIDE/CLAMP is a medical device that received FDA 510(k) clearance on 1991-11-21. The listed applicant is Pilling Co.. The 510(k) number is K914015.

When did CLEMENT-PILLING CHOLANGIOGRAPHY CATH GUIDE/CLAMP receive FDA 510(k) clearance?

CLEMENT-PILLING CHOLANGIOGRAPHY CATH GUIDE/CLAMP received FDA 510(k) clearance on 1991-11-21, under 510(k) number K914015.

Who is the listed applicant for CLEMENT-PILLING CHOLANGIOGRAPHY CATH GUIDE/CLAMP?

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 CLEMENT-PILLING CHOLANGIOGRAPHY CATH GUIDE/CLAMP?

The FDA product code for CLEMENT-PILLING CHOLANGIOGRAPHY CATH GUIDE/CLAMP is GBZ.

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 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.

View all 39 devices →

Related Devices (Code: GBZ)

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.

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