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FDA 510(k)

3-WAY STOPCOCK WITH LUER-LOCK FITTING

K-Number: K770154 · 1977-02-28

ApplicantAmerican Viggo
Decision Date1977-02-28
Product CodeKGZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

3-WAY STOPCOCK WITH LUER-LOCK FITTING is the device name listed in this FDA 510(k) record. The listed applicant is American Viggo. It received FDA 510(k) clearance on 1977-02-28 under 510(k) number K770154. The device is classified under product code KGZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 3-WAY STOPCOCK WITH LUER-LOCK FITTING?

3-WAY STOPCOCK WITH LUER-LOCK FITTING is a medical device that received FDA 510(k) clearance on 1977-02-28. The listed applicant is American Viggo. The 510(k) number is K770154.

When did 3-WAY STOPCOCK WITH LUER-LOCK FITTING receive FDA 510(k) clearance?

3-WAY STOPCOCK WITH LUER-LOCK FITTING received FDA 510(k) clearance on 1977-02-28, under 510(k) number K770154.

Who is the listed applicant for 3-WAY STOPCOCK WITH LUER-LOCK FITTING?

The FDA 510(k) record lists American Viggo as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 3-WAY STOPCOCK WITH LUER-LOCK FITTING?

The FDA product code for 3-WAY STOPCOCK WITH LUER-LOCK FITTING is KGZ.

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Other records listing American Viggo 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.

K771339MALE LUER LOCK PLUGK770528NEEDLE, MEMBRANEK770181I.V. CATHETER PLACEMENT UNITK770174LUER-LOCK EXTENSION SETK770096EPIDURAL BLOCK PROCEDURE PACKK7606794-WAY STOPCOCK W/7CM TUBING,

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Related Devices (Code: KGZ)

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.

K022306AART SILICONE TUBINGAesthetic and Reconstructive Technologies, Inc.K974295BYRON MEDICAL ASPIRATION AND INFILTRATION/IRRIGATION TUBINGByron MedicalK973183WOUND DRAINAGE HOLDERR & D Medical Products, Inc.K955433DURALASTIC SILICONE TUBINGAllied Biomedical Corp.K942315NAVARRE PERCUTANEOUS ACCESS SETNavarre Biomedical , Ltd.K896087PALESTRANT IRRIGATION AND DRAINAGE SETNorth American Instrument Corp.

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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