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FDA 510(k)

ARGON LASER SURGICAL SYSTEM 770

K-Number: K833387 · 1984-04-18

ApplicantCooper Medical Corp.
Decision Date1984-04-18
Product Code
DecisionSubstantially Equivalent

Device Summary

ARGON LASER SURGICAL SYSTEM 770 is the device name listed in this FDA 510(k) record. The listed applicant is Cooper Medical Corp.. It received FDA 510(k) clearance on 1984-04-18 under 510(k) number K833387. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARGON LASER SURGICAL SYSTEM 770?

ARGON LASER SURGICAL SYSTEM 770 is a medical device that received FDA 510(k) clearance on 1984-04-18. The listed applicant is Cooper Medical Corp.. The 510(k) number is K833387.

When did ARGON LASER SURGICAL SYSTEM 770 receive FDA 510(k) clearance?

ARGON LASER SURGICAL SYSTEM 770 received FDA 510(k) clearance on 1984-04-18, under 510(k) number K833387.

Who is the listed applicant for ARGON LASER SURGICAL SYSTEM 770?

The FDA 510(k) record lists Cooper Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

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.

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Other records listing Cooper Medical Corp. 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.

K840144YAG LASER 8000 GASTROINTESTINAL BLEEK833497COOPER MEDICAL MODEL 770K832703ARGON LASER SYS-MODEL 5000K820261MONITOR CO2 LASER SYSTEM

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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