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FDA 510(k)

MILLARD MOUTH GAG

K-Number: K780992 · 1978-08-17

ApplicantNestor Engineering Associates, Inc.
Decision Date1978-08-17
Product CodeKBN
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

MILLARD MOUTH GAG 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 1978-08-17 under 510(k) number K780992. The device is classified under product code KBN. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MILLARD MOUTH GAG?

MILLARD MOUTH GAG is a medical device that received FDA 510(k) clearance on 1978-08-17. The listed applicant is Nestor Engineering Associates, Inc.. The 510(k) number is K780992.

When did MILLARD MOUTH GAG receive FDA 510(k) clearance?

MILLARD MOUTH GAG received FDA 510(k) clearance on 1978-08-17, under 510(k) number K780992.

Who is the listed applicant for MILLARD MOUTH GAG?

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

What is the FDA product code for MILLARD MOUTH GAG?

The FDA product code for MILLARD MOUTH GAG is KBN.

Related Clinical Trials

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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.

K780990STAINLESS STEEL TEMPLATEK780988DEVIN-NESTOR PNEUMATIC TOURNIQUETK780991PARALLEL BLADE MARKERK780989DEVIN-NESTOR SQUARE KNIFE

Related Devices (Code: KBN)

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.

K834540OP-CON SURGICAL INSTRUMENT #9Imm Enterprises , Ltd.K822183MOUTH GAGSKelleher Corp.

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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