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FDA 510(k)

STOCKINETTE, DISPOSABLESURGICAL

K-Number: K782091 · 1979-01-10

ApplicantAnago, Inc.
Decision Date1979-01-10
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STOCKINETTE, DISPOSABLESURGICAL is the device name listed in this FDA 510(k) record. The listed applicant is Anago, Inc.. It received FDA 510(k) clearance on 1979-01-10 under 510(k) number K782091. 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 STOCKINETTE, DISPOSABLESURGICAL?

STOCKINETTE, DISPOSABLESURGICAL is a medical device that received FDA 510(k) clearance on 1979-01-10. The listed applicant is Anago, Inc.. The 510(k) number is K782091.

When did STOCKINETTE, DISPOSABLESURGICAL receive FDA 510(k) clearance?

STOCKINETTE, DISPOSABLESURGICAL received FDA 510(k) clearance on 1979-01-10, under 510(k) number K782091.

Who is the listed applicant for STOCKINETTE, DISPOSABLESURGICAL?

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 STOCKINETTE, DISPOSABLESURGICAL?

The FDA product code for STOCKINETTE, DISPOSABLESURGICAL is KKX.

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Other records listing Anago, Inc. as applicant

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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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