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FDA 510(k)

MALE LUER CONNECTOR & HINGED CAP

K-Number: K820169 · 1982-02-05

ApplicantExtracorporeal Medical Specialities, Inc.
Decision Date1982-02-05
Product CodeFJK
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MALE LUER CONNECTOR & HINGED CAP is the device name listed in this FDA 510(k) record. The listed applicant is Extracorporeal Medical Specialities, Inc.. It received FDA 510(k) clearance on 1982-02-05 under 510(k) number K820169. The device is classified under product code FJK. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MALE LUER CONNECTOR & HINGED CAP?

MALE LUER CONNECTOR & HINGED CAP is a medical device that received FDA 510(k) clearance on 1982-02-05. The listed applicant is Extracorporeal Medical Specialities, Inc.. The 510(k) number is K820169.

When did MALE LUER CONNECTOR & HINGED CAP receive FDA 510(k) clearance?

MALE LUER CONNECTOR & HINGED CAP received FDA 510(k) clearance on 1982-02-05, under 510(k) number K820169.

Who is the listed applicant for MALE LUER CONNECTOR & HINGED CAP?

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

What is the FDA product code for MALE LUER CONNECTOR & HINGED CAP?

The FDA product code for MALE LUER CONNECTOR & HINGED CAP is FJK.

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Other records listing Extracorporeal Medical Specialities, Inc. as applicant

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Related Devices (Code: FJK)

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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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