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FDA 510(k)

ASPIRATOR/IRRIGATOR OR I/A UNIT

K-Number: K820889 · 1982-05-05

ApplicantMid Laboratories, Inc.
Decision Date1982-05-05
Product CodeKYG
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ASPIRATOR/IRRIGATOR OR I/A UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Mid Laboratories, Inc.. It received FDA 510(k) clearance on 1982-05-05 under 510(k) number K820889. The device is classified under product code KYG. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASPIRATOR/IRRIGATOR OR I/A UNIT?

ASPIRATOR/IRRIGATOR OR I/A UNIT is a medical device that received FDA 510(k) clearance on 1982-05-05. The listed applicant is Mid Laboratories, Inc.. The 510(k) number is K820889.

When did ASPIRATOR/IRRIGATOR OR I/A UNIT receive FDA 510(k) clearance?

ASPIRATOR/IRRIGATOR OR I/A UNIT received FDA 510(k) clearance on 1982-05-05, under 510(k) number K820889.

Who is the listed applicant for ASPIRATOR/IRRIGATOR OR I/A UNIT?

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

What is the FDA product code for ASPIRATOR/IRRIGATOR OR I/A UNIT?

The FDA product code for ASPIRATOR/IRRIGATOR OR I/A UNIT is KYG.

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 Mid Laboratories, 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.

K812857CHARLES MICRO PROBE

Related Devices (Code: KYG)

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.

K010353MED-LOGICS DISPOSABLE ALK TUBINGMed-Logics, Inc.K003036TURBO-FLOW INFUSION CANNULA 19 GAGE,20 GAGE,23 GAGE, 25 GAGE, MODEL 101019,101020,101023,101025Retinalabs.ComK993591BLADEWORKS DISPOSABLE ALK TUBINGBlade Works, Inc.K981116SOVEREIGN CATARACT EXTRACTION SYSTEMAllergan, Inc.K980647EYE IRRIGATOR MODEL #2020Eye-Deal Ocular Safety Products, Inc.K974561MOISTAIR FLUID AIR TUBING SETAmerican Medical Devices, 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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