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FDA 510(k)

PRE-VIEW CHOLANGIOGRAPHY CLAMP

K-Number: K973621 · 1997-12-17

ApplicantNashville Surgical Instruments
Decision Date1997-12-17
Product CodeGBZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PRE-VIEW CHOLANGIOGRAPHY CLAMP is the device name listed in this FDA 510(k) record. The listed applicant is Nashville Surgical Instruments. It received FDA 510(k) clearance on 1997-12-17 under 510(k) number K973621. 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 PRE-VIEW CHOLANGIOGRAPHY CLAMP?

PRE-VIEW CHOLANGIOGRAPHY CLAMP is a medical device that received FDA 510(k) clearance on 1997-12-17. The listed applicant is Nashville Surgical Instruments. The 510(k) number is K973621.

When did PRE-VIEW CHOLANGIOGRAPHY CLAMP receive FDA 510(k) clearance?

PRE-VIEW CHOLANGIOGRAPHY CLAMP received FDA 510(k) clearance on 1997-12-17, under 510(k) number K973621.

Who is the listed applicant for PRE-VIEW CHOLANGIOGRAPHY CLAMP?

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

What is the FDA product code for PRE-VIEW CHOLANGIOGRAPHY CLAMP?

The FDA product code for PRE-VIEW CHOLANGIOGRAPHY 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.

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Other records listing Nashville Surgical Instruments 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.

K081366KUMAR T-ANCHORS HERNIA SET

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.

K944790FLEXIBLE LAPAROSCOPIC CHOLANGIOGRAPHY CATHETERApplied Medical ResourcesK942450ENDOPATHEthicon Endo-Surgery, Inc.K932228MICROVASIVE INSURG CHLOANGIOGRAPHIC CATHETERBoston Scientific CorpK926217TERUMO ANGIOGRAPHIC CATHETER FOR LAPOROSCOPIC USETerumo Medical Corp.K926143ANGIOLAPCATH CHOLANGIOGRAPHY KITBd Becton Dickinson Vacutainer Systems PreanalyticK924212STRYKER ENDOSCOPY CHOLANGIOGRAM KITStryker Corp.

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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