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FDA 510(k)

LAPAROMED CHOLANGIOGRAM VACUUM DEVICE

K-Number: K910218 · 1991-04-08

Decision Date1991-04-08
Product CodeGCX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LAPAROMED CHOLANGIOGRAM VACUUM DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Laparomed Corp.. It received FDA 510(k) clearance on 1991-04-08 under 510(k) number K910218. The device is classified under product code GCX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LAPAROMED CHOLANGIOGRAM VACUUM DEVICE?

LAPAROMED CHOLANGIOGRAM VACUUM DEVICE is a medical device that received FDA 510(k) clearance on 1991-04-08. The listed applicant is Laparomed Corp.. The 510(k) number is K910218.

When did LAPAROMED CHOLANGIOGRAM VACUUM DEVICE receive FDA 510(k) clearance?

LAPAROMED CHOLANGIOGRAM VACUUM DEVICE received FDA 510(k) clearance on 1991-04-08, under 510(k) number K910218.

Who is the listed applicant for LAPAROMED CHOLANGIOGRAM VACUUM DEVICE?

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

What is the FDA product code for LAPAROMED CHOLANGIOGRAM VACUUM DEVICE?

The FDA product code for LAPAROMED CHOLANGIOGRAM VACUUM DEVICE is GCX.

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 Laparomed Corp. 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 10 devices →

Related Devices (Code: GCX)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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