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FDA 510(k)

AUTOMATIC SPLICING DEVICE

K-Number: K822025 · 1982-09-09

Decision Date1982-09-09
Product CodeFKX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

AUTOMATIC SPLICING DEVICE 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 1982-09-09 under 510(k) number K822025. The device is classified under product code FKX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTOMATIC SPLICING DEVICE?

AUTOMATIC SPLICING DEVICE is a medical device that received FDA 510(k) clearance on 1982-09-09. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K822025.

When did AUTOMATIC SPLICING DEVICE receive FDA 510(k) clearance?

AUTOMATIC SPLICING DEVICE received FDA 510(k) clearance on 1982-09-09, under 510(k) number K822025.

Who is the listed applicant for AUTOMATIC SPLICING DEVICE?

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 AUTOMATIC SPLICING DEVICE?

The FDA product code for AUTOMATIC SPLICING DEVICE is FKX.

Related Clinical Trials

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.

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.

View all 253 devices →

Related Devices (Code: FKX)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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