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FDA 510(k)

SPHYGMOMANOMETER #1235

K-Number: K771666 · 1977-09-30

ApplicantSears, Roebuck & Co.
Decision Date1977-09-30
Product CodeDXG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SPHYGMOMANOMETER #1235 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 1977-09-30 under 510(k) number K771666. The device is classified under product code DXG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPHYGMOMANOMETER #1235?

SPHYGMOMANOMETER #1235 is a medical device that received FDA 510(k) clearance on 1977-09-30. The listed applicant is Sears, Roebuck & Co.. The 510(k) number is K771666.

When did SPHYGMOMANOMETER #1235 receive FDA 510(k) clearance?

SPHYGMOMANOMETER #1235 received FDA 510(k) clearance on 1977-09-30, under 510(k) number K771666.

Who is the listed applicant for SPHYGMOMANOMETER #1235?

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 SPHYGMOMANOMETER #1235?

The FDA product code for SPHYGMOMANOMETER #1235 is DXG.

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Other records listing Sears, Roebuck & Co. as applicant

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Related Devices (Code: DXG)

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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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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