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FDA 510(k)

PREPARE LOCK

K-Number: K936094 · 1994-02-03

ApplicantPrepare, Inc.
Decision Date1994-02-03
Product CodeCBH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PREPARE LOCK is the device name listed in this FDA 510(k) record. The listed applicant is Prepare, Inc.. It received FDA 510(k) clearance on 1994-02-03 under 510(k) number K936094. The device is classified under product code CBH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PREPARE LOCK?

PREPARE LOCK is a medical device that received FDA 510(k) clearance on 1994-02-03. The listed applicant is Prepare, Inc.. The 510(k) number is K936094.

When did PREPARE LOCK receive FDA 510(k) clearance?

PREPARE LOCK received FDA 510(k) clearance on 1994-02-03, under 510(k) number K936094.

Who is the listed applicant for PREPARE LOCK?

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

What is the FDA product code for PREPARE LOCK?

The FDA product code for PREPARE LOCK is CBH.

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Related Devices (Code: CBH)

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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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