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FDA 510(k)

PARALLEL BLADE MARKER

K-Number: K780991 · 1978-10-03

ApplicantNestor Engineering Associates, Inc.
Decision Date1978-10-03
Product CodeEMF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PARALLEL BLADE MARKER 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 K780991. The device is classified under product code EMF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PARALLEL BLADE MARKER?

PARALLEL BLADE MARKER 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 K780991.

When did PARALLEL BLADE MARKER receive FDA 510(k) clearance?

PARALLEL BLADE MARKER received FDA 510(k) clearance on 1978-10-03, under 510(k) number K780991.

Who is the listed applicant for PARALLEL BLADE MARKER?

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 PARALLEL BLADE MARKER?

The FDA product code for PARALLEL BLADE MARKER is EMF.

Related Clinical Trials

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.

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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 TOURNIQUETK780989DEVIN-NESTOR SQUARE KNIFEK780992MILLARD MOUTH GAG

Related Devices (Code: EMF)

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.

K080133MOUNTABLE ENDOSCOPIC BLADEA.M. Surgical, Inc.K982142MOUNTABLE ENDOSCOPIC KNIFEA.M. Surgical, Inc.K890215MICROSURGICAL SCARIFIERKinetic Medical ProductsK890217MICROSURGICAL KNIVESKinetic Medical ProductsK890214MICROSURGERY RAZOR BLADE HOLDERKinetic Medical ProductsK880094VAN-TEC ENDOPYELOTOMY KNIFEVan-Tec, Inc.

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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