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FDA 510(k)

CONPHAR SUCTION CATHETER-W/0 CONTROL

K-Number: K791253 · 1979-07-30

ApplicantConphar, Inc.
Decision Date1979-07-30
Product CodeBSY
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CONPHAR SUCTION CATHETER-W/0 CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Conphar, Inc.. It received FDA 510(k) clearance on 1979-07-30 under 510(k) number K791253. The device is classified under product code BSY. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONPHAR SUCTION CATHETER-W/0 CONTROL?

CONPHAR SUCTION CATHETER-W/0 CONTROL is a medical device that received FDA 510(k) clearance on 1979-07-30. The listed applicant is Conphar, Inc.. The 510(k) number is K791253.

When did CONPHAR SUCTION CATHETER-W/0 CONTROL receive FDA 510(k) clearance?

CONPHAR SUCTION CATHETER-W/0 CONTROL received FDA 510(k) clearance on 1979-07-30, under 510(k) number K791253.

Who is the listed applicant for CONPHAR SUCTION CATHETER-W/0 CONTROL?

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 SUCTION CATHETER-W/0 CONTROL?

The FDA product code for CONPHAR SUCTION CATHETER-W/0 CONTROL is BSY.

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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: BSY)

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.

K031997MALLINCKRODT DAR TY-CARE / TY-CARE EXEL CLOSED SUCTION SYSTEMMallinckrodt Dar S.R.L.K992902AMBU HAND POWER SUCTION PUMPAmbu, Inc.K982945DUAL PURPOSE CLOSED CATHETERSpirit Medical Systems, Inc.K981910SUCTION CATHETERNi-Med, Inc.K972258HI-CARE CLOSED SUCTION SYSTEMMallinckrodt MedicalK973199AMSINO SUCTION CATHETERAmsino Intl., Inc.

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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