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FDA 510(k)

ANEROID SPHYGMOMANOMETER, DOCTOR TYPE

K-Number: K901506 · 1990-05-09

ApplicantYamasu Co. , Ltd.
Decision Date1990-05-09
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ANEROID SPHYGMOMANOMETER, DOCTOR TYPE is the device name listed in this FDA 510(k) record. The listed applicant is Yamasu Co. , Ltd.. It received FDA 510(k) clearance on 1990-05-09 under 510(k) number K901506. The device is classified under product code DXQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANEROID SPHYGMOMANOMETER, DOCTOR TYPE?

ANEROID SPHYGMOMANOMETER, DOCTOR TYPE is a medical device that received FDA 510(k) clearance on 1990-05-09. The listed applicant is Yamasu Co. , Ltd.. The 510(k) number is K901506.

When did ANEROID SPHYGMOMANOMETER, DOCTOR TYPE receive FDA 510(k) clearance?

ANEROID SPHYGMOMANOMETER, DOCTOR TYPE received FDA 510(k) clearance on 1990-05-09, under 510(k) number K901506.

Who is the listed applicant for ANEROID SPHYGMOMANOMETER, DOCTOR TYPE?

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

What is the FDA product code for ANEROID SPHYGMOMANOMETER, DOCTOR TYPE?

The FDA product code for ANEROID SPHYGMOMANOMETER, DOCTOR TYPE is DXQ.

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 Yamasu Co. , Ltd. 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.

K884420HOME BLOOD PRESSURE KIT, ANEROID

Related Devices (Code: DXQ)

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.

K254287Medline Reusable Blood Pressure CuffMedline Industries, LPK260747YP-710T Series NIBP Cuff;YP-840T Series Disposable CuffNihon Kohden CorporationK253089NIBP Cuff (BCS-112, BCS-212, BCS-312, BCS-412, BCS-512, BCS-612, BCS-712, BCS-122, BCS-222, BCS-322, BCS-422, BCS-522, BCS-622, BCS-722, BCD-112, BCD-212, BCD-312, BCD-412, BCD-512, BCD-612, BCD-712, BCD-122, BCD-222, BCD-322, BCD-422, BCD-522, BCD-622, BCD-722)Shenzhen Best Electronics Co., Ltd.K253964Disposable Neonatal NIBP Cuff (U1681S-C51N)Unimed Medical Supplies, Inc.K251745Welch Allyn FlexiPort Blood Pressure Cuffs (FlexiPort Blood Pressure Cuffs)Baxter Healthcare CorporationK250765AViTA Arm Type Blood Pressure Monitor CuffAvita Corporation

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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