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FDA 510(k)

EFFNER CAUTERY INSTRUMENTS

K-Number: K875260 · 1988-06-06

Decision Date1988-06-06
Product CodeHQP
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

EFFNER CAUTERY INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Effner and Spreine Co.. It received FDA 510(k) clearance on 1988-06-06 under 510(k) number K875260. The device is classified under product code HQP. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EFFNER CAUTERY INSTRUMENTS?

EFFNER CAUTERY INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1988-06-06. The listed applicant is Effner and Spreine Co.. The 510(k) number is K875260.

When did EFFNER CAUTERY INSTRUMENTS receive FDA 510(k) clearance?

EFFNER CAUTERY INSTRUMENTS received FDA 510(k) clearance on 1988-06-06, under 510(k) number K875260.

Who is the listed applicant for EFFNER CAUTERY INSTRUMENTS?

The FDA 510(k) record lists Effner and Spreine Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EFFNER CAUTERY INSTRUMENTS?

The FDA product code for EFFNER CAUTERY INSTRUMENTS is HQP.

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.

Other records listing Effner and Spreine Co. 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.

Related Devices (Code: HQP)

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.

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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