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FDA 510(k)

AGAR 3K NEUROMUSCULAR STIMULATOR

K-Number: K882386 · 1989-10-18

ApplicantSolcoor, Inc.
Decision Date1989-10-18
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

AGAR 3K NEUROMUSCULAR STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Solcoor, Inc.. It received FDA 510(k) clearance on 1989-10-18 under 510(k) number K882386. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AGAR 3K NEUROMUSCULAR STIMULATOR?

AGAR 3K NEUROMUSCULAR STIMULATOR is a medical device that received FDA 510(k) clearance on 1989-10-18. The listed applicant is Solcoor, Inc.. The 510(k) number is K882386.

When did AGAR 3K NEUROMUSCULAR STIMULATOR receive FDA 510(k) clearance?

AGAR 3K NEUROMUSCULAR STIMULATOR received FDA 510(k) clearance on 1989-10-18, under 510(k) number K882386.

Who is the listed applicant for AGAR 3K NEUROMUSCULAR STIMULATOR?

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

What is the FDA product code for AGAR 3K NEUROMUSCULAR STIMULATOR?

The FDA product code for AGAR 3K NEUROMUSCULAR STIMULATOR is IPF.

Related Clinical Trials

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.

Other records listing Solcoor, 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.

View all 7 devices →

Related Devices (Code: IPF)

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.

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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