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FDA 510(k)

LEUR TIP CAP, VLT CAP(TM)

K-Number: K945454 · 1995-04-14

Decision Date1995-04-14
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LEUR TIP CAP, VLT CAP(TM) is the device name listed in this FDA 510(k) record. The listed applicant is Martell Medical Products, Inc.. It received FDA 510(k) clearance on 1995-04-14 under 510(k) number K945454. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LEUR TIP CAP, VLT CAP(TM)?

LEUR TIP CAP, VLT CAP(TM) is a medical device that received FDA 510(k) clearance on 1995-04-14. The listed applicant is Martell Medical Products, Inc.. The 510(k) number is K945454.

When did LEUR TIP CAP, VLT CAP(TM) receive FDA 510(k) clearance?

LEUR TIP CAP, VLT CAP(TM) received FDA 510(k) clearance on 1995-04-14, under 510(k) number K945454.

Who is the listed applicant for LEUR TIP CAP, VLT CAP(TM)?

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

What is the FDA product code for LEUR TIP CAP, VLT CAP(TM)?

The FDA product code for LEUR TIP CAP, VLT CAP(TM) is JKA.

Other records listing Martell 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.

View all 7 devices →

Related Devices (Code: JKA)

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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