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FDA 510(k)

LOCKBOX

K-Number: K942161 · 1994-08-02

ApplicantPharmacia Deltec, Inc.
Decision Date1994-08-02
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent - Subject to Tracking Reg.

Device Summary

LOCKBOX is the device name listed in this FDA 510(k) record. The listed applicant is Pharmacia Deltec, Inc.. It received FDA 510(k) clearance on 1994-08-02 under 510(k) number K942161. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent - Subject to Tracking Reg..

Frequently Asked Questions

What is the LOCKBOX?

LOCKBOX is a medical device that received FDA 510(k) clearance on 1994-08-02. The listed applicant is Pharmacia Deltec, Inc.. The 510(k) number is K942161.

When did LOCKBOX receive FDA 510(k) clearance?

LOCKBOX received FDA 510(k) clearance on 1994-08-02, under 510(k) number K942161.

Who is the listed applicant for LOCKBOX?

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

What is the FDA product code for LOCKBOX?

The FDA product code for LOCKBOX is FRN.

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Other records listing Pharmacia Deltec, Inc. as applicant

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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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