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FDA 510(k)

STAINLESS STEEL TEMPLATE

K-Number: K780990 · 1978-10-03

ApplicantNestor Engineering Associates, Inc.
Decision Date1978-10-03
Product Code
DecisionSubstantially Equivalent

Device Summary

STAINLESS STEEL TEMPLATE is the device name listed in this FDA 510(k) record. The listed applicant is Nestor Engineering Associates, Inc.. It received FDA 510(k) clearance on 1978-10-03 under 510(k) number K780990. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STAINLESS STEEL TEMPLATE?

STAINLESS STEEL TEMPLATE is a medical device that received FDA 510(k) clearance on 1978-10-03. The listed applicant is Nestor Engineering Associates, Inc.. The 510(k) number is K780990.

When did STAINLESS STEEL TEMPLATE receive FDA 510(k) clearance?

STAINLESS STEEL TEMPLATE received FDA 510(k) clearance on 1978-10-03, under 510(k) number K780990.

Who is the listed applicant for STAINLESS STEEL TEMPLATE?

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

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Other records listing Nestor Engineering Associates, 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.

K780988DEVIN-NESTOR PNEUMATIC TOURNIQUETK780991PARALLEL BLADE MARKERK780989DEVIN-NESTOR SQUARE KNIFEK780992MILLARD MOUTH GAG

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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