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FDA 510(k)

CATHETER, DOVER SUCTION W/ GLOVE

K-Number: K760427 · 1976-09-09

ApplicantWill Ross Co.
Decision Date1976-09-09
Product CodeBSY
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CATHETER, DOVER SUCTION W/ GLOVE is the device name listed in this FDA 510(k) record. The listed applicant is Will Ross Co.. It received FDA 510(k) clearance on 1976-09-09 under 510(k) number K760427. 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 CATHETER, DOVER SUCTION W/ GLOVE?

CATHETER, DOVER SUCTION W/ GLOVE is a medical device that received FDA 510(k) clearance on 1976-09-09. The listed applicant is Will Ross Co.. The 510(k) number is K760427.

When did CATHETER, DOVER SUCTION W/ GLOVE receive FDA 510(k) clearance?

CATHETER, DOVER SUCTION W/ GLOVE received FDA 510(k) clearance on 1976-09-09, under 510(k) number K760427.

Who is the listed applicant for CATHETER, DOVER SUCTION W/ GLOVE?

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

What is the FDA product code for CATHETER, DOVER SUCTION W/ GLOVE?

The FDA product code for CATHETER, DOVER SUCTION W/ GLOVE is BSY.

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Other records listing Will Ross Co. 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.

K780850SEARLE NEONATAL OXYGEN PROBEK771561DOVER URINE METERK771132KENWOOD BIOLOGICAL STEOILIZ. INDICATORK770607TRACTION HARNESSK770608WALKING AIDK770609TABLE, MASSAGE & TREATMHNT, FIXED HEIGHT

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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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