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FDA 510(k)

CUFF-M

K-Number: K921997 · 1992-07-23

ApplicantLorin Medical, Inc.
Decision Date1992-07-23
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CUFF-M is the device name listed in this FDA 510(k) record. The listed applicant is Lorin Medical, Inc.. It received FDA 510(k) clearance on 1992-07-23 under 510(k) number K921997. 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 CUFF-M?

CUFF-M is a medical device that received FDA 510(k) clearance on 1992-07-23. The listed applicant is Lorin Medical, Inc.. The 510(k) number is K921997.

When did CUFF-M receive FDA 510(k) clearance?

CUFF-M received FDA 510(k) clearance on 1992-07-23, under 510(k) number K921997.

Who is the listed applicant for CUFF-M?

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

What is the FDA product code for CUFF-M?

The FDA product code for CUFF-M is DXQ.

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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