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FDA 510(k)

DUPONT PREP FOUR-SOLVENT RETROFIT KIT

K-Number: K851393 · 1985-07-12

ApplicantE.I. Dupont DE Nemours & Co., Inc.
Decision Date1985-07-12
Product CodeJJH
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DUPONT PREP FOUR-SOLVENT RETROFIT KIT 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 1985-07-12 under 510(k) number K851393. The device is classified under product code JJH. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUPONT PREP FOUR-SOLVENT RETROFIT KIT?

DUPONT PREP FOUR-SOLVENT RETROFIT KIT is a medical device that received FDA 510(k) clearance on 1985-07-12. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K851393.

When did DUPONT PREP FOUR-SOLVENT RETROFIT KIT receive FDA 510(k) clearance?

DUPONT PREP FOUR-SOLVENT RETROFIT KIT received FDA 510(k) clearance on 1985-07-12, under 510(k) number K851393.

Who is the listed applicant for DUPONT PREP FOUR-SOLVENT RETROFIT KIT?

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 DUPONT PREP FOUR-SOLVENT RETROFIT KIT?

The FDA product code for DUPONT PREP FOUR-SOLVENT RETROFIT KIT is JJH.

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

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Related Devices (Code: JJH)

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.

K113731ESENSOR RESPIRATORY VIRAL PANELClinical Micro Sensors, Inc.K960298VIVASPIN 4 10,000 MWVivascience, Inc.K943965VIVAPORE 10Vivascience, Inc.K943966VIVAPORE 2Vivascience, Inc.K941326ULTRAFREE-CLMillipore Corp.K935496NANOSEP N10Intersep , Ltd.

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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