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FDA 510(k)

ANAGO STERILE PRODUCTS; STOCKINETTES

K-Number: K813097 · 1982-03-10

ApplicantAnago, Inc.
Decision Date1982-03-10
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ANAGO STERILE PRODUCTS; STOCKINETTES is the device name listed in this FDA 510(k) record. The listed applicant is Anago, Inc.. It received FDA 510(k) clearance on 1982-03-10 under 510(k) number K813097. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANAGO STERILE PRODUCTS; STOCKINETTES?

ANAGO STERILE PRODUCTS; STOCKINETTES is a medical device that received FDA 510(k) clearance on 1982-03-10. The listed applicant is Anago, Inc.. The 510(k) number is K813097.

When did ANAGO STERILE PRODUCTS; STOCKINETTES receive FDA 510(k) clearance?

ANAGO STERILE PRODUCTS; STOCKINETTES received FDA 510(k) clearance on 1982-03-10, under 510(k) number K813097.

Who is the listed applicant for ANAGO STERILE PRODUCTS; STOCKINETTES?

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

What is the FDA product code for ANAGO STERILE PRODUCTS; STOCKINETTES?

The FDA product code for ANAGO STERILE PRODUCTS; STOCKINETTES is KKX.

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Other records listing Anago, Inc. as applicant

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K925659U.C.E.Z. LENS CLEANER KITK930161ANAGO SPINAL ANESTHESIA TRAYK926590ANAGO DISPOSABLE INSTANT COLD PACKK926137ANAGO FEM-COOL/FEM-COOL PETITEK926589ANAGO WARM PACKK920615ANAGO CONTINUOUS EPIDURAL ANESTHESIA TRAY/KIT

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Related Devices (Code: KKX)

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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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