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FDA 510(k)

PULSAMAT MODEL 1050

K-Number: K830906 · 1983-06-15

ApplicantFerring Laboratories, Inc.
Decision Date1983-06-15
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PULSAMAT MODEL 1050 is the device name listed in this FDA 510(k) record. The listed applicant is Ferring Laboratories, Inc.. It received FDA 510(k) clearance on 1983-06-15 under 510(k) number K830906. 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 PULSAMAT MODEL 1050?

PULSAMAT MODEL 1050 is a medical device that received FDA 510(k) clearance on 1983-06-15. The listed applicant is Ferring Laboratories, Inc.. The 510(k) number is K830906.

When did PULSAMAT MODEL 1050 receive FDA 510(k) clearance?

PULSAMAT MODEL 1050 received FDA 510(k) clearance on 1983-06-15, under 510(k) number K830906.

Who is the listed applicant for PULSAMAT MODEL 1050?

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

What is the FDA product code for PULSAMAT MODEL 1050?

The FDA product code for PULSAMAT MODEL 1050 is FRN.

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Other records listing Ferring Laboratories, 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.

K881759BT-1 INFUSION PUMP

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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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