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FDA 510(k)

DIRECT CURRENT BONE GROWTH STIM. AN. PAD

K-Number: K810271 · 1981-02-19

ApplicantAndover Medical, Inc.
Decision Date1981-02-19
Product Code
DecisionSubstantially Equivalent

Device Summary

DIRECT CURRENT BONE GROWTH STIM. AN. PAD is the device name listed in this FDA 510(k) record. The listed applicant is Andover Medical, Inc.. It received FDA 510(k) clearance on 1981-02-19 under 510(k) number K810271. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIRECT CURRENT BONE GROWTH STIM. AN. PAD?

DIRECT CURRENT BONE GROWTH STIM. AN. PAD is a medical device that received FDA 510(k) clearance on 1981-02-19. The listed applicant is Andover Medical, Inc.. The 510(k) number is K810271.

When did DIRECT CURRENT BONE GROWTH STIM. AN. PAD receive FDA 510(k) clearance?

DIRECT CURRENT BONE GROWTH STIM. AN. PAD received FDA 510(k) clearance on 1981-02-19, under 510(k) number K810271.

Who is the listed applicant for DIRECT CURRENT BONE GROWTH STIM. AN. PAD?

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

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Other records listing Andover Medical, Inc. as applicant

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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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