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FDA 510(k)

VENT-O2-CATH

K-Number: K760371 · 1976-08-13

ApplicantDryden Corp.
Decision Date1976-08-13
Product CodeBSY
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VENT-O2-CATH is the device name listed in this FDA 510(k) record. The listed applicant is Dryden Corp.. It received FDA 510(k) clearance on 1976-08-13 under 510(k) number K760371. 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 VENT-O2-CATH?

VENT-O2-CATH is a medical device that received FDA 510(k) clearance on 1976-08-13. The listed applicant is Dryden Corp.. The 510(k) number is K760371.

When did VENT-O2-CATH receive FDA 510(k) clearance?

VENT-O2-CATH received FDA 510(k) clearance on 1976-08-13, under 510(k) number K760371.

Who is the listed applicant for VENT-O2-CATH?

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

What is the FDA product code for VENT-O2-CATH?

The FDA product code for VENT-O2-CATH is BSY.

Other records listing Dryden Corp. 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.

K880923PATIENT VENTILATOR ISOLATORK880769BREATHING CIRCUIT W/HEATED WIREK882285NONREBREATHING CIRCUITK873928UNIVERSAL TOURNIQUETK873927REUSEABLE BREATHING TUBESK870859BAG-TAIL BLEED VALVE

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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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