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FDA 510(k)

M.R. ASSOC. ALLIGATOR GRASPONG FORCEPS

K-Number: K800967 · 1980-05-08

Decision Date1980-05-08
Product CodeOCZ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

M.R. ASSOC. ALLIGATOR GRASPONG FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Mr Associates, Inc.. It received FDA 510(k) clearance on 1980-05-08 under 510(k) number K800967. The device is classified under product code OCZ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the M.R. ASSOC. ALLIGATOR GRASPONG FORCEPS?

M.R. ASSOC. ALLIGATOR GRASPONG FORCEPS is a medical device that received FDA 510(k) clearance on 1980-05-08. The listed applicant is Mr Associates, Inc.. The 510(k) number is K800967.

When did M.R. ASSOC. ALLIGATOR GRASPONG FORCEPS receive FDA 510(k) clearance?

M.R. ASSOC. ALLIGATOR GRASPONG FORCEPS received FDA 510(k) clearance on 1980-05-08, under 510(k) number K800967.

Who is the listed applicant for M.R. ASSOC. ALLIGATOR GRASPONG FORCEPS?

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

What is the FDA product code for M.R. ASSOC. ALLIGATOR GRASPONG FORCEPS?

The FDA product code for M.R. ASSOC. ALLIGATOR GRASPONG FORCEPS is OCZ.

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 Mr 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.

View all 15 devices →

Related Devices (Code: OCZ)

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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