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FDA 510(k)

CEMENT EXTRACTION INSTRUMENTATION

K-Number: K822554 · 1982-09-14

ApplicantSurgi-Quip Inc.U
Decision Date1982-09-14
Product Code
DecisionSubstantially Equivalent

Device Summary

CEMENT EXTRACTION INSTRUMENTATION is the device name listed in this FDA 510(k) record. The listed applicant is Surgi-Quip Inc.U. It received FDA 510(k) clearance on 1982-09-14 under 510(k) number K822554. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CEMENT EXTRACTION INSTRUMENTATION?

CEMENT EXTRACTION INSTRUMENTATION is a medical device that received FDA 510(k) clearance on 1982-09-14. The listed applicant is Surgi-Quip Inc.U. The 510(k) number is K822554.

When did CEMENT EXTRACTION INSTRUMENTATION receive FDA 510(k) clearance?

CEMENT EXTRACTION INSTRUMENTATION received FDA 510(k) clearance on 1982-09-14, under 510(k) number K822554.

Who is the listed applicant for CEMENT EXTRACTION INSTRUMENTATION?

The FDA 510(k) record lists Surgi-Quip Inc.U as the applicant. This does not by itself establish the device manufacturer.

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Other records listing Surgi-Quip Inc.U 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.

K841116MOBILE OPHTHALMIC OPERATING TABLEK841115CHARLES/MCINTYRE GIANT BREAK TABLEK840004WEE BAG O'MERCURYK832887ELECTRONIC UNITK822427SELF-CONTAINED MOBILE OPHTHAL. OPER. .K822428SURGI-QUIP MICROSCOPE STAND

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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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