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FDA 510(k)

RIZA BAND STRETCHER (RBS)-60000

K-Number: K001236 · 2000-07-17

ApplicantR-Med, Inc.
Decision Date2000-07-17
Product CodeFHN
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

RIZA BAND STRETCHER (RBS)-60000 is the device name listed in this FDA 510(k) record. The listed applicant is R-Med, Inc.. It received FDA 510(k) clearance on 2000-07-17 under 510(k) number K001236. The device is classified under product code FHN. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RIZA BAND STRETCHER (RBS)-60000?

RIZA BAND STRETCHER (RBS)-60000 is a medical device that received FDA 510(k) clearance on 2000-07-17. The listed applicant is R-Med, Inc.. The 510(k) number is K001236.

When did RIZA BAND STRETCHER (RBS)-60000 receive FDA 510(k) clearance?

RIZA BAND STRETCHER (RBS)-60000 received FDA 510(k) clearance on 2000-07-17, under 510(k) number K001236.

Who is the listed applicant for RIZA BAND STRETCHER (RBS)-60000?

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

What is the FDA product code for RIZA BAND STRETCHER (RBS)-60000?

The FDA product code for RIZA BAND STRETCHER (RBS)-60000 is FHN.

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Other records listing R-Med, Inc. 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.

K953360R-MED ABDOMINAL WALL ELEVATORK954882RIZA-RIBE NEEDLE (MODIFICATION)K953441RIZA-RIBE NEEDLEK950108R-MED MINI-RETRACTORK942411R-MED DISPOSABLE PLUGK945637R-MED MOTORIZED LAPAROSCOPIC HANDLE

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Related Devices (Code: FHN)

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.

K213223Multi-Band LigatorBeijing Zksk Technology Co., Ltd.K172985Ligation DeviceLeo Medical Co., Ltd.K131282NEXUS HEMORRHOID LIGATORInx MedicalK093497THD BANDYThd SpaK091519HAEMOBAND MULTI-LIGATORHaemoband Surgical, Ltd.K070881LEM HEMORRHOIDAL LIGATOR, MODELS A.5650, A.5660Sapimed S.P.A.

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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