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FDA 510(k)

DENVER PLEURO-PERITONEAL SHUNT

K-Number: K880570 · 1988-06-20

ApplicantCodman & Shurtleff, Inc.
Decision Date1988-06-20
Product CodeKPM
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DENVER PLEURO-PERITONEAL SHUNT is the device name listed in this FDA 510(k) record. The listed applicant is Codman & Shurtleff, Inc.. It received FDA 510(k) clearance on 1988-06-20 under 510(k) number K880570. The device is classified under product code KPM. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DENVER PLEURO-PERITONEAL SHUNT?

DENVER PLEURO-PERITONEAL SHUNT is a medical device that received FDA 510(k) clearance on 1988-06-20. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K880570.

When did DENVER PLEURO-PERITONEAL SHUNT receive FDA 510(k) clearance?

DENVER PLEURO-PERITONEAL SHUNT received FDA 510(k) clearance on 1988-06-20, under 510(k) number K880570.

Who is the listed applicant for DENVER PLEURO-PERITONEAL SHUNT?

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

What is the FDA product code for DENVER PLEURO-PERITONEAL SHUNT?

The FDA product code for DENVER PLEURO-PERITONEAL SHUNT is KPM.

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Other records listing Codman & Shurtleff, Inc. as applicant

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Related Devices (Code: KPM)

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.

K231096Automatic Continuous Effusion Shunt (ACES) System ACES SystemPleural Dynamics, Inc.K170405BD Curve Ascites ShuntCare FusionK012235DENVER PLEURAL EFFUSION SHUNT AND DENVER PLEURAL EFFUSION SHUNT WITH EXTERNAL PUMP CHAMBERDenver Biomedical, Inc.K011862DENVER ASCITES SHUNT AND PERCUTANEOUS ACCESS KIT WITH ASCITIES SHUNTDenver Biomedical, Inc.K011020DENVER PLEURAL EFFUSION SHUNT WITH EXTERNAL PUMP CHAMBERDenver Biomedicals, Inc.K003451DENVER PAK W/ DOUBLE-VALVE ASCITES SHUNT,DENVER PAK W/ SINGLE-VALVED ASCITES SHUNT, DENVER PAK, DOUBLED-VALVED ASCITES TDenver Biomedicals, Inc.

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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