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FDA 510(k)

PERISTALTIC INFUSION PUMP (2100,2101)

K-Number: K760718 · 1976-10-14

ApplicantExtracorporeal Medical Specialities, Inc.
Decision Date1976-10-14
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PERISTALTIC INFUSION PUMP (2100,2101) is the device name listed in this FDA 510(k) record. The listed applicant is Extracorporeal Medical Specialities, Inc.. It received FDA 510(k) clearance on 1976-10-14 under 510(k) number K760718. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERISTALTIC INFUSION PUMP (2100,2101)?

PERISTALTIC INFUSION PUMP (2100,2101) is a medical device that received FDA 510(k) clearance on 1976-10-14. The listed applicant is Extracorporeal Medical Specialities, Inc.. The 510(k) number is K760718.

When did PERISTALTIC INFUSION PUMP (2100,2101) receive FDA 510(k) clearance?

PERISTALTIC INFUSION PUMP (2100,2101) received FDA 510(k) clearance on 1976-10-14, under 510(k) number K760718.

Who is the listed applicant for PERISTALTIC INFUSION PUMP (2100,2101)?

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

What is the FDA product code for PERISTALTIC INFUSION PUMP (2100,2101)?

The FDA product code for PERISTALTIC INFUSION PUMP (2100,2101) is FRN.

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Other records listing Extracorporeal Medical Specialities, Inc. as applicant

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Related Devices (Code: FRN)

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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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