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FDA 510(k)

CATHETER/HEMOSTATIC/GERIATRIC

K-Number: K780062 · 1978-02-14

ApplicantKendall Research Center
Decision Date1978-02-14
Product CodeEZL
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CATHETER/HEMOSTATIC/GERIATRIC is the device name listed in this FDA 510(k) record. The listed applicant is Kendall Research Center. It received FDA 510(k) clearance on 1978-02-14 under 510(k) number K780062. The device is classified under product code EZL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CATHETER/HEMOSTATIC/GERIATRIC?

CATHETER/HEMOSTATIC/GERIATRIC is a medical device that received FDA 510(k) clearance on 1978-02-14. The listed applicant is Kendall Research Center. The 510(k) number is K780062.

When did CATHETER/HEMOSTATIC/GERIATRIC receive FDA 510(k) clearance?

CATHETER/HEMOSTATIC/GERIATRIC received FDA 510(k) clearance on 1978-02-14, under 510(k) number K780062.

Who is the listed applicant for CATHETER/HEMOSTATIC/GERIATRIC?

The FDA 510(k) record lists Kendall Research Center as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CATHETER/HEMOSTATIC/GERIATRIC?

The FDA product code for CATHETER/HEMOSTATIC/GERIATRIC is EZL.

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Other records listing Kendall Research Center 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.

K802225TENDER-SORB DRAIN SPONGESK781357T.E.D. SEQUENTIAL COMPRESSION SLEEVESK780408MICRONET LIGHT DRESSING SPONGEK780120ANESTHESIA TRAY, CAUDALK772133URINE SPECIMEN COLLECTING DEVICEK772134SYRINGE, IRRIGATION, PRE-FILLED

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Related Devices (Code: EZL)

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.

K260756TraumaGuard Intra-Abdominal Pressure-Sensing System (000-0221)Sentinel Medical Technologies,K262056Rusch Latex Gold Foley CatheterTeleflex Medical Sdn. Bhd.K252537Rusch SoftSimplastic Foley CathetersTeleflex Medical Sdn. Bhd.K243011Silicone Urethral Catheter (Silicone Urethral Catheter)Guangdong Ecan Medical Co., Ltd.K241424InnoCare Specialty Foley CatheterInnocare Urologics, LLCK232469Rüsch Latex Gold Foley CatheterTeleflexmedical, Inc.

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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