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FDA 510(k)

MOORE MANUFACTURE MODEL-MHBTL

K-Number: K923912 · 1993-02-12

ApplicantMoore Mfg., Inc.
Decision Date1993-02-12
Product CodeILK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MOORE MANUFACTURE MODEL-MHBTL is the device name listed in this FDA 510(k) record. The listed applicant is Moore Mfg., Inc.. It received FDA 510(k) clearance on 1993-02-12 under 510(k) number K923912. The device is classified under product code ILK. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOORE MANUFACTURE MODEL-MHBTL?

MOORE MANUFACTURE MODEL-MHBTL is a medical device that received FDA 510(k) clearance on 1993-02-12. The listed applicant is Moore Mfg., Inc.. The 510(k) number is K923912.

When did MOORE MANUFACTURE MODEL-MHBTL receive FDA 510(k) clearance?

MOORE MANUFACTURE MODEL-MHBTL received FDA 510(k) clearance on 1993-02-12, under 510(k) number K923912.

Who is the listed applicant for MOORE MANUFACTURE MODEL-MHBTL?

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

What is the FDA product code for MOORE MANUFACTURE MODEL-MHBTL?

The FDA product code for MOORE MANUFACTURE MODEL-MHBTL is ILK.

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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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