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FDA 510(k)

DISPOSABLE STERILE LAP SPONGE

K-Number: K802980 · 1980-12-19

ApplicantAnago, Inc.
Decision Date1980-12-19
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE STERILE LAP SPONGE is the device name listed in this FDA 510(k) record. The listed applicant is Anago, Inc.. It received FDA 510(k) clearance on 1980-12-19 under 510(k) number K802980. 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 DISPOSABLE STERILE LAP SPONGE?

DISPOSABLE STERILE LAP SPONGE is a medical device that received FDA 510(k) clearance on 1980-12-19. The listed applicant is Anago, Inc.. The 510(k) number is K802980.

When did DISPOSABLE STERILE LAP SPONGE receive FDA 510(k) clearance?

DISPOSABLE STERILE LAP SPONGE received FDA 510(k) clearance on 1980-12-19, under 510(k) number K802980.

Who is the listed applicant for DISPOSABLE STERILE LAP SPONGE?

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 DISPOSABLE STERILE LAP SPONGE?

The FDA product code for DISPOSABLE STERILE LAP SPONGE is KKX.

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Other records listing Anago, Inc. as applicant

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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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