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FDA 510(k)

BLOOD PRESSURE, DIGITAL MODEL #2153

K-Number: K781701 · 1978-12-04

ApplicantSears, Roebuck & Co.
Decision Date1978-12-04
Product CodeDSK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BLOOD PRESSURE, DIGITAL MODEL #2153 is the device name listed in this FDA 510(k) record. The listed applicant is Sears, Roebuck & Co.. It received FDA 510(k) clearance on 1978-12-04 under 510(k) number K781701. 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 BLOOD PRESSURE, DIGITAL MODEL #2153?

BLOOD PRESSURE, DIGITAL MODEL #2153 is a medical device that received FDA 510(k) clearance on 1978-12-04. The listed applicant is Sears, Roebuck & Co.. The 510(k) number is K781701.

When did BLOOD PRESSURE, DIGITAL MODEL #2153 receive FDA 510(k) clearance?

BLOOD PRESSURE, DIGITAL MODEL #2153 received FDA 510(k) clearance on 1978-12-04, under 510(k) number K781701.

Who is the listed applicant for BLOOD PRESSURE, DIGITAL MODEL #2153?

The FDA 510(k) record lists Sears, Roebuck & Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BLOOD PRESSURE, DIGITAL MODEL #2153?

The FDA product code for BLOOD PRESSURE, DIGITAL MODEL #2153 is DSK.

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Other records listing Sears, Roebuck & 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.

K810635ELECTRODE BLOOD PRESSURE MONITORK800778DIGITAL ELECTRONIC B.P. MONITOR 2155K800072DIGITAL ELECTRONIC EXERCISER/PULSE MTR.K780986DIGITAL BLOOD PRESSURE MONITORK771666SPHYGMOMANOMETER #1235

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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