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FDA 510(k)

L-CATH CONNECTOR ASSEMBLY

K-Number: K940198 · 1994-12-15

ApplicantLuther Medical Products, Inc.
Decision Date1994-12-15
Product CodeGCD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

L-CATH CONNECTOR ASSEMBLY is the device name listed in this FDA 510(k) record. The listed applicant is Luther Medical Products, Inc.. It received FDA 510(k) clearance on 1994-12-15 under 510(k) number K940198. The device is classified under product code GCD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the L-CATH CONNECTOR ASSEMBLY?

L-CATH CONNECTOR ASSEMBLY is a medical device that received FDA 510(k) clearance on 1994-12-15. The listed applicant is Luther Medical Products, Inc.. The 510(k) number is K940198.

When did L-CATH CONNECTOR ASSEMBLY receive FDA 510(k) clearance?

L-CATH CONNECTOR ASSEMBLY received FDA 510(k) clearance on 1994-12-15, under 510(k) number K940198.

Who is the listed applicant for L-CATH CONNECTOR ASSEMBLY?

The FDA 510(k) record lists Luther Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for L-CATH CONNECTOR ASSEMBLY?

The FDA product code for L-CATH CONNECTOR ASSEMBLY is GCD.

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Other records listing Luther Medical Products, Inc. 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.

K982797BLUNT T-PEEL INTRODUCER MODEL NUMBER PE-16PICB, PE-18PICB, PE-20PICB, PE-24PICBK980090ONECATH, L-CATH CATHETER SYSTEM, MODEL OC-(16-22 GA., 5CM-60CM)K974543L-CATH MODIFIED SELDINGER TECHNIQUE INSERTION/CATHETER EXCHANGE KIT PE-MST24-24 GA. KIT, L-CATH MODIFIED SELDINGERK942103L-CATH CATHETER SYSTEM - PORT L-CATHK930473ONECATH L-CATH CATHETER SYSTEMK925236L CATH(R) CATHETER SYSTEM

View all 17 devices →

Related Devices (Code: GCD)

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.

K952470ACTI-FLEX LOW, MEDIUM, RESCARE I, RESCARE II.R-Group Intl.K863446ANGIOMED HIGH PRESSURE CONNECTORSAngiomed U.S., Inc.K851196INCISION DRAINSil-Med Corp.K851921Y CONNECTORSil-Med Corp.K760382CONNECTORSB. Braun InstrumentsK760524CATHETER CONNECTOR, ARGYLE TUBINGSherwood Medical Industries

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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