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FDA 510(k)

SPONGE COUNTER

K-Number: K926225 · 1993-03-05

ApplicantAmerican Medical Manufacturer, Inc.
Decision Date1993-03-05
Product CodeFWZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SPONGE COUNTER is the device name listed in this FDA 510(k) record. The listed applicant is American Medical Manufacturer, Inc.. It received FDA 510(k) clearance on 1993-03-05 under 510(k) number K926225. The device is classified under product code FWZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPONGE COUNTER?

SPONGE COUNTER is a medical device that received FDA 510(k) clearance on 1993-03-05. The listed applicant is American Medical Manufacturer, Inc.. The 510(k) number is K926225.

When did SPONGE COUNTER receive FDA 510(k) clearance?

SPONGE COUNTER received FDA 510(k) clearance on 1993-03-05, under 510(k) number K926225.

Who is the listed applicant for SPONGE COUNTER?

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

What is the FDA product code for SPONGE COUNTER?

The FDA product code for SPONGE COUNTER is FWZ.

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Related Devices (Code: FWZ)

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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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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