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FDA 510(k)

RANGE OF CROCODILE ACTION INSTRUMENTS

K-Number: K873934 · 1987-12-17

Decision Date1987-12-17
Product CodeGZX
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

RANGE OF CROCODILE ACTION INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Downs Surgical , Ltd.. It received FDA 510(k) clearance on 1987-12-17 under 510(k) number K873934. The device is classified under product code GZX. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RANGE OF CROCODILE ACTION INSTRUMENTS?

RANGE OF CROCODILE ACTION INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1987-12-17. The listed applicant is Downs Surgical , Ltd.. The 510(k) number is K873934.

When did RANGE OF CROCODILE ACTION INSTRUMENTS receive FDA 510(k) clearance?

RANGE OF CROCODILE ACTION INSTRUMENTS received FDA 510(k) clearance on 1987-12-17, under 510(k) number K873934.

Who is the listed applicant for RANGE OF CROCODILE ACTION INSTRUMENTS?

The FDA 510(k) record lists Downs Surgical , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RANGE OF CROCODILE ACTION INSTRUMENTS?

The FDA product code for RANGE OF CROCODILE ACTION INSTRUMENTS is GZX.

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 Downs Surgical , Ltd. 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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Related Devices (Code: GZX)

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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