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FDA 510(k)

REMINGTON MEDICAL DISPOSABLE EXTENSION CABLE FAS-LOC FL-601

K-Number: K940467 · 1994-11-01

Decision Date1994-11-01
Product CodeDTE
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

REMINGTON MEDICAL DISPOSABLE EXTENSION CABLE FAS-LOC FL-601 is the device name listed in this FDA 510(k) record. The listed applicant is Remington Medical, Inc.. It received FDA 510(k) clearance on 1994-11-01 under 510(k) number K940467. The device is classified under product code DTE. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REMINGTON MEDICAL DISPOSABLE EXTENSION CABLE FAS-LOC FL-601?

REMINGTON MEDICAL DISPOSABLE EXTENSION CABLE FAS-LOC FL-601 is a medical device that received FDA 510(k) clearance on 1994-11-01. The listed applicant is Remington Medical, Inc.. The 510(k) number is K940467.

When did REMINGTON MEDICAL DISPOSABLE EXTENSION CABLE FAS-LOC FL-601 receive FDA 510(k) clearance?

REMINGTON MEDICAL DISPOSABLE EXTENSION CABLE FAS-LOC FL-601 received FDA 510(k) clearance on 1994-11-01, under 510(k) number K940467.

Who is the listed applicant for REMINGTON MEDICAL DISPOSABLE EXTENSION CABLE FAS-LOC FL-601?

The FDA 510(k) record lists Remington Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for REMINGTON MEDICAL DISPOSABLE EXTENSION CABLE FAS-LOC FL-601?

The FDA product code for REMINGTON MEDICAL DISPOSABLE EXTENSION CABLE FAS-LOC FL-601 is DTE.

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 Remington Medical, 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 18 devices →

Related Devices (Code: DTE)

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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