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FDA 510(k)

RELIEVED REINFORCED CUP

K-Number: K820539 · 1982-03-15

ApplicantBiomet, Inc.
Decision Date1982-03-15
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RELIEVED REINFORCED CUP is the device name listed in this FDA 510(k) record. The listed applicant is Biomet, Inc.. It received FDA 510(k) clearance on 1982-03-15 under 510(k) number K820539. 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 RELIEVED REINFORCED CUP?

RELIEVED REINFORCED CUP is a medical device that received FDA 510(k) clearance on 1982-03-15. The listed applicant is Biomet, Inc.. The 510(k) number is K820539.

When did RELIEVED REINFORCED CUP receive FDA 510(k) clearance?

RELIEVED REINFORCED CUP received FDA 510(k) clearance on 1982-03-15, under 510(k) number K820539.

Who is the listed applicant for RELIEVED REINFORCED CUP?

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

What is the FDA product code for RELIEVED REINFORCED CUP?

The FDA product code for RELIEVED REINFORCED CUP is DXQ.

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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

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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