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FDA 510(k)

UC-2000 UTERINE CATHERIZATION SYSTEM

K-Number: K791633 · 1979-09-17

ApplicantLife Support, Inc.
Decision Date1979-09-17
Product CodeHFO
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

UC-2000 UTERINE CATHERIZATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Life Support, Inc.. It received FDA 510(k) clearance on 1979-09-17 under 510(k) number K791633. The device is classified under product code HFO. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UC-2000 UTERINE CATHERIZATION SYSTEM?

UC-2000 UTERINE CATHERIZATION SYSTEM is a medical device that received FDA 510(k) clearance on 1979-09-17. The listed applicant is Life Support, Inc.. The 510(k) number is K791633.

When did UC-2000 UTERINE CATHERIZATION SYSTEM receive FDA 510(k) clearance?

UC-2000 UTERINE CATHERIZATION SYSTEM received FDA 510(k) clearance on 1979-09-17, under 510(k) number K791633.

Who is the listed applicant for UC-2000 UTERINE CATHERIZATION SYSTEM?

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

What is the FDA product code for UC-2000 UTERINE CATHERIZATION SYSTEM?

The FDA product code for UC-2000 UTERINE CATHERIZATION SYSTEM is HFO.

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Other records listing Life Support, 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.

K801984FE-3000 FETAL ELECTRODE, SPIRAL SYSTEM

Related Devices (Code: HFO)

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.

K973850ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY #M007Alexander Mfg. Co.K943989LAPAROSCOPIC/ENDOSCOPIC INSTRUEMENTGabris Surgical Corp.K780487FETAL MONITORING SYSTEMSonicaid, Inc.

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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