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FDA 510(k)

POLLENEX DIGITAL SPHYGMOMANOMETER BP-2000

K-Number: K844396 · 1985-04-18

ApplicantAssociated Mills, Inc.
Decision Date1985-04-18
Product CodeDSK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

POLLENEX DIGITAL SPHYGMOMANOMETER BP-2000 is the device name listed in this FDA 510(k) record. The listed applicant is Associated Mills, Inc.. It received FDA 510(k) clearance on 1985-04-18 under 510(k) number K844396. The device is classified under product code DSK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POLLENEX DIGITAL SPHYGMOMANOMETER BP-2000?

POLLENEX DIGITAL SPHYGMOMANOMETER BP-2000 is a medical device that received FDA 510(k) clearance on 1985-04-18. The listed applicant is Associated Mills, Inc.. The 510(k) number is K844396.

When did POLLENEX DIGITAL SPHYGMOMANOMETER BP-2000 receive FDA 510(k) clearance?

POLLENEX DIGITAL SPHYGMOMANOMETER BP-2000 received FDA 510(k) clearance on 1985-04-18, under 510(k) number K844396.

Who is the listed applicant for POLLENEX DIGITAL SPHYGMOMANOMETER BP-2000?

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

What is the FDA product code for POLLENEX DIGITAL SPHYGMOMANOMETER BP-2000?

The FDA product code for POLLENEX DIGITAL SPHYGMOMANOMETER BP-2000 is DSK.

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Other records listing Associated Mills, 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.

K901459DS60 TOOTHBRUSH SANITIZERK872327WHIRLPOOL AERATOR WB700, WB800, WB900, WB975K871661WH150 ROOM HUMIDIFIERK862041WM10, WM20, WM30 POWER MASSAGERK862042SH20, SH30 & SH50 ULTRASONIC HUMIDIFIERK844397POLLENEX DIGITAL SPHYGMOMANOMETER BP-4000

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Related Devices (Code: DSK)

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.

K231586Endophys Blood Pressure Monitor model BPM-30Endophys Technologies, LLCK160945Endophys Blood Pressure MonitorEndophys Holdings, LLCK080670MODIFICATION TO SPHYGMOCOR CARDIOVASCULAR MANAGEMENT SYSTEMAtcor MedicalK070795SPHYGMOCOR CARDIOVASCULAR MANAGEMENT SYSTEMAtcor Medical Pty, Ltd.K033738MONITORING SYSTEM, MODEL ARGUS PB-2200Schiller AGK021517ABP FOR WINDOWSRozinn Electronics, 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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