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FDA 510(k)

ELECTRO NEUROMUSCULAR STIMULATOR, MODEL NMS-DIGITAL

K-Number: K010749 · 2001-09-28

ApplicantBiomedical Life Systems, Inc.
Decision Date2001-09-28
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ELECTRO NEUROMUSCULAR STIMULATOR, MODEL NMS-DIGITAL is the device name listed in this FDA 510(k) record. The listed applicant is Biomedical Life Systems, Inc.. It received FDA 510(k) clearance on 2001-09-28 under 510(k) number K010749. 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 ELECTRO NEUROMUSCULAR STIMULATOR, MODEL NMS-DIGITAL?

ELECTRO NEUROMUSCULAR STIMULATOR, MODEL NMS-DIGITAL is a medical device that received FDA 510(k) clearance on 2001-09-28. The listed applicant is Biomedical Life Systems, Inc.. The 510(k) number is K010749.

When did ELECTRO NEUROMUSCULAR STIMULATOR, MODEL NMS-DIGITAL receive FDA 510(k) clearance?

ELECTRO NEUROMUSCULAR STIMULATOR, MODEL NMS-DIGITAL received FDA 510(k) clearance on 2001-09-28, under 510(k) number K010749.

Who is the listed applicant for ELECTRO NEUROMUSCULAR STIMULATOR, MODEL NMS-DIGITAL?

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

What is the FDA product code for ELECTRO NEUROMUSCULAR STIMULATOR, MODEL NMS-DIGITAL?

The FDA product code for ELECTRO NEUROMUSCULAR STIMULATOR, MODEL NMS-DIGITAL is IPF.

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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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