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FDA 510(k)

DIRECT READOUT MODULE ACCESSORY

K-Number: K861412 · 1986-05-23

ApplicantE.I. Dupont DE Nemours & Co., Inc.
Decision Date1986-05-23
Product CodeJQP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DIRECT READOUT MODULE ACCESSORY is the device name listed in this FDA 510(k) record. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. It received FDA 510(k) clearance on 1986-05-23 under 510(k) number K861412. The device is classified under product code JQP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIRECT READOUT MODULE ACCESSORY?

DIRECT READOUT MODULE ACCESSORY is a medical device that received FDA 510(k) clearance on 1986-05-23. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K861412.

When did DIRECT READOUT MODULE ACCESSORY receive FDA 510(k) clearance?

DIRECT READOUT MODULE ACCESSORY received FDA 510(k) clearance on 1986-05-23, under 510(k) number K861412.

Who is the listed applicant for DIRECT READOUT MODULE ACCESSORY?

The FDA 510(k) record lists E.I. Dupont DE Nemours & Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIRECT READOUT MODULE ACCESSORY?

The FDA product code for DIRECT READOUT MODULE ACCESSORY is JQP.

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Other records listing E.I. Dupont DE Nemours & Co., Inc. as applicant

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Related Devices (Code: JQP)

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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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