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FDA 510(k)

ACA DATA MATE ACCESSORY

K-Number: K760739 · 1976-11-16

ApplicantE.I. Dupont DE Nemours & Co., Inc.
Decision Date1976-11-16
Product CodeJQP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ACA DATA MATE 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 1976-11-16 under 510(k) number K760739. 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 ACA DATA MATE ACCESSORY?

ACA DATA MATE ACCESSORY is a medical device that received FDA 510(k) clearance on 1976-11-16. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K760739.

When did ACA DATA MATE ACCESSORY receive FDA 510(k) clearance?

ACA DATA MATE ACCESSORY received FDA 510(k) clearance on 1976-11-16, under 510(k) number K760739.

Who is the listed applicant for ACA DATA MATE 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 ACA DATA MATE ACCESSORY?

The FDA product code for ACA DATA MATE ACCESSORY is JQP.

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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.

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Related Devices (Code: JQP)

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.

K113007BIONIME DIABETES MANAGEMENT SYSTEM VI.0Bionime CorporationK983468FASTTAKE ADAPTER, MODEL # P/N 020-072-01Selfcare, Inc.K964460THE ROBOLITEShai Syg Motion and Innovations, Ltd.K953652PRENVAL IBase Ten Systems, Inc.K934111MR7000 WITH TIME MANAGER SOFTWARE (TMS)Dynatech Laboratories, Inc.K923316EXPRESSO CARTRIDGEBio-Rad Laboratories, Inc.

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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