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FDA 510(k)

5 IN 1 CONNECTOR

K-Number: K861757 · 1986-06-06

ApplicantJackson Plastics, Inc.
Decision Date1986-06-06
Product CodeGAZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

5 IN 1 CONNECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Jackson Plastics, Inc.. It received FDA 510(k) clearance on 1986-06-06 under 510(k) number K861757. The device is classified under product code GAZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 5 IN 1 CONNECTOR?

5 IN 1 CONNECTOR is a medical device that received FDA 510(k) clearance on 1986-06-06. The listed applicant is Jackson Plastics, Inc.. The 510(k) number is K861757.

When did 5 IN 1 CONNECTOR receive FDA 510(k) clearance?

5 IN 1 CONNECTOR received FDA 510(k) clearance on 1986-06-06, under 510(k) number K861757.

Who is the listed applicant for 5 IN 1 CONNECTOR?

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

What is the FDA product code for 5 IN 1 CONNECTOR?

The FDA product code for 5 IN 1 CONNECTOR is GAZ.

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Related Devices (Code: GAZ)

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.

K952605SUCTION/IRRIGATOR TUBING KITSurgical Laser Technologies, Inc.K945978TUBING, NONINVASIVEEndoscopic Technologies, Inc.K930512SUCTION/IRRIGATION Y TUBING SET W/TRUMPET VALVESCore Dynamics, Inc.K911865NORTEC CONNECTING TUBE SETNorth American Sterilization & Packaging Co.K910471MEDID-VAC CLEAR NONCONDUCTIVE CONNECTING TUBEBaxter Healthcare CorpK910170MAXI-FLOW SUCTION SET 12 FT.Adler Instrument Co.

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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