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FDA 510(k)

SINGLE USE NON-CONDUCTIVE CIRC. DISCON

K-Number: K821667 · 1982-06-24

ApplicantVital Signs, Inc.
Decision Date1982-06-24
Product CodeCAP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SINGLE USE NON-CONDUCTIVE CIRC. DISCON is the device name listed in this FDA 510(k) record. The listed applicant is Vital Signs, Inc.. It received FDA 510(k) clearance on 1982-06-24 under 510(k) number K821667. The device is classified under product code CAP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SINGLE USE NON-CONDUCTIVE CIRC. DISCON?

SINGLE USE NON-CONDUCTIVE CIRC. DISCON is a medical device that received FDA 510(k) clearance on 1982-06-24. The listed applicant is Vital Signs, Inc.. The 510(k) number is K821667.

When did SINGLE USE NON-CONDUCTIVE CIRC. DISCON receive FDA 510(k) clearance?

SINGLE USE NON-CONDUCTIVE CIRC. DISCON received FDA 510(k) clearance on 1982-06-24, under 510(k) number K821667.

Who is the listed applicant for SINGLE USE NON-CONDUCTIVE CIRC. DISCON?

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

What is the FDA product code for SINGLE USE NON-CONDUCTIVE CIRC. DISCON?

The FDA product code for SINGLE USE NON-CONDUCTIVE CIRC. DISCON is CAP.

Related Clinical Trials

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.

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Other records listing Vital Signs, 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.

K112902ENFLOW IV FLUID WARMERK041309IMASK TMK030985BREAS PV 10I CPAP SYSTEM, MODEL PV 10IK022402DISPOSABLE PRESSURE MANOMETERK021315SURE-LOKK002454BREAS HA50 HUMIDIFIER, MODEL HA50

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Related Devices (Code: CAP)

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.

K201666SINGLE USE MANOMETERFlexicare Medical Limited.K182292VORTRAN APM-PlusVortran Medical Technology 1, Inc.K180510NS 120P-TRS Airway Pressure GaugeInstrumentation Industries, Inc.K172284NAPA LP-15 Airway Pressure MonitorDrw Medical, LLCK153733VORTRAN ManometerVortran Medical Technology 1, Inc.K122627GIO DIGITAL PRESSURE GUAGESGalemed 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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