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FDA 510(k)

DIGITAL ELECTRONIC EXERCISER/PULSE MTR.

K-Number: K800072 · 1980-01-28

ApplicantSears, Roebuck & Co.
Decision Date1980-01-28
Product CodeISD
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

DIGITAL ELECTRONIC EXERCISER/PULSE MTR. 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 1980-01-28 under 510(k) number K800072. The device is classified under product code ISD. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIGITAL ELECTRONIC EXERCISER/PULSE MTR.?

DIGITAL ELECTRONIC EXERCISER/PULSE MTR. is a medical device that received FDA 510(k) clearance on 1980-01-28. The listed applicant is Sears, Roebuck & Co.. The 510(k) number is K800072.

When did DIGITAL ELECTRONIC EXERCISER/PULSE MTR. receive FDA 510(k) clearance?

DIGITAL ELECTRONIC EXERCISER/PULSE MTR. received FDA 510(k) clearance on 1980-01-28, under 510(k) number K800072.

Who is the listed applicant for DIGITAL ELECTRONIC EXERCISER/PULSE MTR.?

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 DIGITAL ELECTRONIC EXERCISER/PULSE MTR.?

The FDA product code for DIGITAL ELECTRONIC EXERCISER/PULSE MTR. is ISD.

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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 2155K781701BLOOD PRESSURE, DIGITAL MODEL #2153K780986DIGITAL BLOOD PRESSURE MONITORK771666SPHYGMOMANOMETER #1235

Related Devices (Code: ISD)

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.

K202979MR Egometer Pedal, MR Ergometer Push/Pull, MR Ergometer Up/Down, MR Ergometer Dorsal Ankle Flex, MR Ergometer Pedal UltraLode B.V.K183296REAL Immersive SystemPenumbra, Inc.K112121ERGOSELECT/GEErgoline GmbHK080545ACTITRAINERActigraph, LLCK053078ERGOSELECT 100 K/P, ERGOSELECT 200 K/PErgoline GmbHK990866QUINTON MEDTRACK CR PLUS TREADMILLQuinton, 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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