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FDA 510(k)

DUPONT PREP OD EXTRACTION CARTRIDE

K-Number: K830692 · 1983-04-05

ApplicantE.I. Dupont DE Nemours & Co., Inc.
Decision Date1983-04-05
Product CodeDJY
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DUPONT PREP OD EXTRACTION CARTRIDE 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 1983-04-05 under 510(k) number K830692. The device is classified under product code DJY. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUPONT PREP OD EXTRACTION CARTRIDE?

DUPONT PREP OD EXTRACTION CARTRIDE is a medical device that received FDA 510(k) clearance on 1983-04-05. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K830692.

When did DUPONT PREP OD EXTRACTION CARTRIDE receive FDA 510(k) clearance?

DUPONT PREP OD EXTRACTION CARTRIDE received FDA 510(k) clearance on 1983-04-05, under 510(k) number K830692.

Who is the listed applicant for DUPONT PREP OD EXTRACTION CARTRIDE?

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 OD EXTRACTION CARTRIDE?

The FDA product code for DUPONT PREP OD EXTRACTION CARTRIDE is DJY.

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

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.

K951851ALLIANCE CYTOMEGALOVIRUS IMMEDIATE EARLY ANTIGEN DIRECT IMMUNOFLUORESCENCE ASSAYK953724CRONEX RADIATION THERAPY CASSETTEK953725CRONEX RADIATION THERAPY VERIFICATION CASSETTEK951441DUPONT ACA DIGOXIN (DGN A) METHODK950137URINE BARBITURATES SCREEN FLEX(TM) REAGENT CARTRIDGEK950136URINE OPIATES SCREEN FLEX(TM) REAGENT CARTRIDGE

View all 253 devices →

Related Devices (Code: DJY)

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.

K890113THE CDI(R) SYSTEM 400Cardiovascular Devices, Inc.K883615LIQUID CHROMATOGRAPHY COLUMNS 5-7070/71/72/73Supelco, Inc.K881361SOLID PHASE EXTRACTION TUBESSupelco, Inc.K850963DUPONT PREP TYPE SI EXTRACITON CARTRIDGEE.I. Dupont DE Nemours & Co., Inc.K840985TRISACRYL GF 05 & TRISACRYL GF 2000Lkb Instruments, Inc.K832198HC40/HC75 PREPACKED COLUMSHamilton Co.

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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