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FDA 510(k)

COOPER MEDICAL MODEL 770

K-Number: K833497 · 1984-04-17

ApplicantCooper Medical Corp.
Decision Date1984-04-17
Product CodeLLF
DecisionSubstantially Equivalent

Device Summary

COOPER MEDICAL MODEL 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 1984-04-17 under 510(k) number K833497. The device is classified under product code LLF. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COOPER MEDICAL MODEL 770?

COOPER MEDICAL MODEL 770 is a medical device that received FDA 510(k) clearance on 1984-04-17. The listed applicant is Cooper Medical Corp.. The 510(k) number is K833497.

When did COOPER MEDICAL MODEL 770 receive FDA 510(k) clearance?

COOPER MEDICAL MODEL 770 received FDA 510(k) clearance on 1984-04-17, under 510(k) number K833497.

Who is the listed applicant for COOPER MEDICAL MODEL 770?

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

What is the FDA product code for COOPER MEDICAL MODEL 770?

The FDA product code for COOPER MEDICAL MODEL 770 is LLF.

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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 BLEEK833387ARGON LASER SURGICAL SYSTEM 770K832703ARGON LASER SYS-MODEL 5000K820261MONITOR CO2 LASER SYSTEM

Related Devices (Code: LLF)

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.

K870773ENDOCOAGULATOR MODELS 5, 8 & 20 ARGON LASERHgm, Inc.K864610CILAS YM 101 ND:YAG LASER FOR NEUROLOGICAL USEInframed, Inc.K860977MODEL 545-45 FOR NEUROLOGICAL SURGICAL APPLICATIONBritt Corp., Inc.

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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