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FDA 510(k)

THORNTON ANTERIOR CHAMBER IRRIGATOR

K-Number: K771732 · 1977-09-28

ApplicantConcept, Inc.
Decision Date1977-09-28
Product CodeGBQ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

THORNTON ANTERIOR CHAMBER IRRIGATOR is the device name listed in this FDA 510(k) record. The listed applicant is Concept, Inc.. It received FDA 510(k) clearance on 1977-09-28 under 510(k) number K771732. The device is classified under product code GBQ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THORNTON ANTERIOR CHAMBER IRRIGATOR?

THORNTON ANTERIOR CHAMBER IRRIGATOR is a medical device that received FDA 510(k) clearance on 1977-09-28. The listed applicant is Concept, Inc.. The 510(k) number is K771732.

When did THORNTON ANTERIOR CHAMBER IRRIGATOR receive FDA 510(k) clearance?

THORNTON ANTERIOR CHAMBER IRRIGATOR received FDA 510(k) clearance on 1977-09-28, under 510(k) number K771732.

Who is the listed applicant for THORNTON ANTERIOR CHAMBER IRRIGATOR?

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

What is the FDA product code for THORNTON ANTERIOR CHAMBER IRRIGATOR?

The FDA product code for THORNTON ANTERIOR CHAMBER IRRIGATOR is GBQ.

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Other records listing Concept, Inc. as applicant

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K912640CONCEPT ENDOSTEAL FIXATION DEVICEK912957CONCEPT MICROMILLK896648CONCEPT UNICOMPARTMENTAL KNEE SYSTEMK894929STAPLE FIXATION SYSTEMK892376INTRAVISION(TM) ARTHROSCOPE SYSTEM (ADD'L APPLI.)K891109PANDA(R) NEEDLE CATHETER JEJUNOSTOMY TUBE

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Related Devices (Code: GBQ)

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.

K941356MICROFLOW IRRIGATION SYSTEMJedmed Instrument Co.K921464CAT.#40100, 40102, 40104 & 40106 YANKAUER SUCT INTTrinity Laboratories, Inc.K882647GESCO CATHETERIZATION TRAYGesco Intl., Inc.K874596PERFORATED SOAKING TUBESpecialty Medical Products Co.K873097PROCEDUAL CHANGES/ASSEMBLY PROCESS FOR PLUS PAKSIpax, Inc.K872787MODIFIED CURLCATHQuinton, Inc.

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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