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FDA 510(k)

SPONGE COUNTER BAGS

K-Number: K791434 · 1979-10-09

Decision Date1979-10-09
Product CodeKDC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SPONGE COUNTER BAGS is the device name listed in this FDA 510(k) record. The listed applicant is Medicare Industries, Inc.. It received FDA 510(k) clearance on 1979-10-09 under 510(k) number K791434. The device is classified under product code KDC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPONGE COUNTER BAGS?

SPONGE COUNTER BAGS is a medical device that received FDA 510(k) clearance on 1979-10-09. The listed applicant is Medicare Industries, Inc.. The 510(k) number is K791434.

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

SPONGE COUNTER BAGS received FDA 510(k) clearance on 1979-10-09, under 510(k) number K791434.

Who is the listed applicant for SPONGE COUNTER BAGS?

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

What is the FDA product code for SPONGE COUNTER BAGS?

The FDA product code for SPONGE COUNTER BAGS is KDC.

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.

Other records listing Medicare Industries, 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.

View all 7 devices →

Related Devices (Code: KDC)

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.

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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