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FDA 510(k)

SYMTEX GAUZE PADS (1'S) AND SYMTEX GAUZE SPONGES STERILE 2'S AND STERILE 10'S

K-Number: K991215 · 1999-06-11

Decision Date1999-06-11
Product CodeEFQ
DecisionSubstantially Equivalent

Device Summary

SYMTEX GAUZE PADS (1'S) AND SYMTEX GAUZE SPONGES STERILE 2'S AND STERILE 10'S is the device name listed in this FDA 510(k) record. The listed applicant is Symtex Healthcare Corp.. It received FDA 510(k) clearance on 1999-06-11 under 510(k) number K991215. The device is classified under product code EFQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYMTEX GAUZE PADS (1'S) AND SYMTEX GAUZE SPONGES STERILE 2'S AND STERILE 10'S?

SYMTEX GAUZE PADS (1'S) AND SYMTEX GAUZE SPONGES STERILE 2'S AND STERILE 10'S is a medical device that received FDA 510(k) clearance on 1999-06-11. The listed applicant is Symtex Healthcare Corp.. The 510(k) number is K991215.

When did SYMTEX GAUZE PADS (1'S) AND SYMTEX GAUZE SPONGES STERILE 2'S AND STERILE 10'S receive FDA 510(k) clearance?

SYMTEX GAUZE PADS (1'S) AND SYMTEX GAUZE SPONGES STERILE 2'S AND STERILE 10'S received FDA 510(k) clearance on 1999-06-11, under 510(k) number K991215.

Who is the listed applicant for SYMTEX GAUZE PADS (1'S) AND SYMTEX GAUZE SPONGES STERILE 2'S AND STERILE 10'S?

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

What is the FDA product code for SYMTEX GAUZE PADS (1'S) AND SYMTEX GAUZE SPONGES STERILE 2'S AND STERILE 10'S?

The FDA product code for SYMTEX GAUZE PADS (1'S) AND SYMTEX GAUZE SPONGES STERILE 2'S AND STERILE 10'S is EFQ.

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.

Related Devices (Code: EFQ)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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