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FDA 510(k)

MONTGOMERY NERVE STIMULATOR

K-Number: K880720 · 1988-05-20

ApplicantBoston Medical Products, Inc.
Decision Date1988-05-20
Product CodeETN
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

MONTGOMERY NERVE STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Boston Medical Products, Inc.. It received FDA 510(k) clearance on 1988-05-20 under 510(k) number K880720. The device is classified under product code ETN. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MONTGOMERY NERVE STIMULATOR?

MONTGOMERY NERVE STIMULATOR is a medical device that received FDA 510(k) clearance on 1988-05-20. The listed applicant is Boston Medical Products, Inc.. The 510(k) number is K880720.

When did MONTGOMERY NERVE STIMULATOR receive FDA 510(k) clearance?

MONTGOMERY NERVE STIMULATOR received FDA 510(k) clearance on 1988-05-20, under 510(k) number K880720.

Who is the listed applicant for MONTGOMERY NERVE STIMULATOR?

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

What is the FDA product code for MONTGOMERY NERVE STIMULATOR?

The FDA product code for MONTGOMERY NERVE STIMULATOR is ETN.

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Other records listing Boston Medical Products, Inc. as applicant

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Related Devices (Code: ETN)

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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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