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FDA 510(k)

FORAMATRON APICAL FORAMEN LOCATOR

K-Number: K811995 · 1981-09-21

ApplicantParker Laboratories, Inc.
Decision Date1981-09-21
Product Code
DecisionSubstantially Equivalent

Device Summary

FORAMATRON APICAL FORAMEN LOCATOR is the device name listed in this FDA 510(k) record. The listed applicant is Parker Laboratories, Inc.. It received FDA 510(k) clearance on 1981-09-21 under 510(k) number K811995. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FORAMATRON APICAL FORAMEN LOCATOR?

FORAMATRON APICAL FORAMEN LOCATOR is a medical device that received FDA 510(k) clearance on 1981-09-21. The listed applicant is Parker Laboratories, Inc.. The 510(k) number is K811995.

When did FORAMATRON APICAL FORAMEN LOCATOR receive FDA 510(k) clearance?

FORAMATRON APICAL FORAMEN LOCATOR received FDA 510(k) clearance on 1981-09-21, under 510(k) number K811995.

Who is the listed applicant for FORAMATRON APICAL FORAMEN LOCATOR?

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

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Other records listing Parker Laboratories, 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.

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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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