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FDA 510(k)

CONPHAR ADAPT-CONNECTS STERILE, NONSTE.

K-Number: K791806 · 1979-09-21

ApplicantConphar, Inc.
Decision Date1979-09-21
Product CodeKGZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CONPHAR ADAPT-CONNECTS STERILE, NONSTE. is the device name listed in this FDA 510(k) record. The listed applicant is Conphar, Inc.. It received FDA 510(k) clearance on 1979-09-21 under 510(k) number K791806. 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 CONPHAR ADAPT-CONNECTS STERILE, NONSTE.?

CONPHAR ADAPT-CONNECTS STERILE, NONSTE. is a medical device that received FDA 510(k) clearance on 1979-09-21. The listed applicant is Conphar, Inc.. The 510(k) number is K791806.

When did CONPHAR ADAPT-CONNECTS STERILE, NONSTE. receive FDA 510(k) clearance?

CONPHAR ADAPT-CONNECTS STERILE, NONSTE. received FDA 510(k) clearance on 1979-09-21, under 510(k) number K791806.

Who is the listed applicant for CONPHAR ADAPT-CONNECTS STERILE, NONSTE.?

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

What is the FDA product code for CONPHAR ADAPT-CONNECTS STERILE, NONSTE.?

The FDA product code for CONPHAR ADAPT-CONNECTS STERILE, NONSTE. is KGZ.

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Other records listing Conphar, 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.

K821825CONPHAR SILICONE FEEDING TUBEK821295OLSEN HEGAR NEEDLE HOLDERSK821289MAYO-HEGAR NEEDLE HOLDERK821354CONPHAR MAYO HEGAR NEEDLE HOLDERK821298BACKHAUS CLAMP, 3 1/2K821290LITTAUER SCISSORS 5 1/2

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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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