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FDA 510(k)

TRIANGULAR SPONGES

K-Number: K953088 · 1995-09-14

Decision Date1995-09-14
Product CodeGDY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TRIANGULAR SPONGES is the device name listed in this FDA 510(k) record. The listed applicant is Medical Perspectives Corp.. It received FDA 510(k) clearance on 1995-09-14 under 510(k) number K953088. 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 TRIANGULAR SPONGES?

TRIANGULAR SPONGES is a medical device that received FDA 510(k) clearance on 1995-09-14. The listed applicant is Medical Perspectives Corp.. The 510(k) number is K953088.

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

TRIANGULAR SPONGES received FDA 510(k) clearance on 1995-09-14, under 510(k) number K953088.

Who is the listed applicant for TRIANGULAR SPONGES?

The FDA 510(k) record lists Medical Perspectives Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TRIANGULAR SPONGES?

The FDA product code for TRIANGULAR 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 Medical Perspectives Corp. 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: 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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