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FDA 510(k)

MEDCO-SONIC NQ-2000

K-Number: K860099 · 1986-04-09

ApplicantMedco Products, Co., Inc.
Decision Date1986-04-09
Product CodeIMI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MEDCO-SONIC NQ-2000 is the device name listed in this FDA 510(k) record. The listed applicant is Medco Products, Co., Inc.. It received FDA 510(k) clearance on 1986-04-09 under 510(k) number K860099. The device is classified under product code IMI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDCO-SONIC NQ-2000?

MEDCO-SONIC NQ-2000 is a medical device that received FDA 510(k) clearance on 1986-04-09. The listed applicant is Medco Products, Co., Inc.. The 510(k) number is K860099.

When did MEDCO-SONIC NQ-2000 receive FDA 510(k) clearance?

MEDCO-SONIC NQ-2000 received FDA 510(k) clearance on 1986-04-09, under 510(k) number K860099.

Who is the listed applicant for MEDCO-SONIC NQ-2000?

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

What is the FDA product code for MEDCO-SONIC NQ-2000?

The FDA product code for MEDCO-SONIC NQ-2000 is IMI.

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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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