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FDA 510(k)

SPECIALTY SPONGES

K-Number: K920355 · 1992-08-06

Decision Date1992-08-06
Product CodeGDY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SPECIALTY SPONGES is the device name listed in this FDA 510(k) record. The listed applicant is Ultracell Medical Technologies, Inc.. It received FDA 510(k) clearance on 1992-08-06 under 510(k) number K920355. The device is classified under product code GDY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPECIALTY SPONGES?

SPECIALTY SPONGES is a medical device that received FDA 510(k) clearance on 1992-08-06. The listed applicant is Ultracell Medical Technologies, Inc.. The 510(k) number is K920355.

When did SPECIALTY SPONGES receive FDA 510(k) clearance?

SPECIALTY SPONGES received FDA 510(k) clearance on 1992-08-06, under 510(k) number K920355.

Who is the listed applicant for SPECIALTY SPONGES?

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

What is the FDA product code for SPECIALTY SPONGES?

The FDA product code for SPECIALTY SPONGES is GDY.

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 Ultracell Medical Technologies, 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 24 devices →

Related Devices (Code: GDY)

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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