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FDA 510(k)

MOORE SECURE CAP

K-Number: K931042 · 1994-04-13

Decision Date1994-04-13
Product CodeLYU
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MOORE SECURE CAP is the device name listed in this FDA 510(k) record. The listed applicant is Kerma Medical Products, Inc.. It received FDA 510(k) clearance on 1994-04-13 under 510(k) number K931042. The device is classified under product code LYU. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOORE SECURE CAP?

MOORE SECURE CAP is a medical device that received FDA 510(k) clearance on 1994-04-13. The listed applicant is Kerma Medical Products, Inc.. The 510(k) number is K931042.

When did MOORE SECURE CAP receive FDA 510(k) clearance?

MOORE SECURE CAP received FDA 510(k) clearance on 1994-04-13, under 510(k) number K931042.

Who is the listed applicant for MOORE SECURE CAP?

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

What is the FDA product code for MOORE SECURE CAP?

The FDA product code for MOORE SECURE CAP is LYU.

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 Kerma 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.

Related Devices (Code: LYU)

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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