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FDA 510(k)

MALE LUER LOCK PLUGS

K-Number: K810921 · 1981-05-21

ApplicantProcedure Products, Inc.
Decision Date1981-05-21
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MALE LUER LOCK PLUGS is the device name listed in this FDA 510(k) record. The listed applicant is Procedure Products, Inc.. It received FDA 510(k) clearance on 1981-05-21 under 510(k) number K810921. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MALE LUER LOCK PLUGS?

MALE LUER LOCK PLUGS is a medical device that received FDA 510(k) clearance on 1981-05-21. The listed applicant is Procedure Products, Inc.. The 510(k) number is K810921.

When did MALE LUER LOCK PLUGS receive FDA 510(k) clearance?

MALE LUER LOCK PLUGS received FDA 510(k) clearance on 1981-05-21, under 510(k) number K810921.

Who is the listed applicant for MALE LUER LOCK PLUGS?

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

What is the FDA product code for MALE LUER LOCK PLUGS?

The FDA product code for MALE LUER LOCK PLUGS is FPA.

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Other records listing Procedure Products, Inc. as applicant

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Related Devices (Code: FPA)

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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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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