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FDA 510(k)

MEDSPEC PACKING GAUZE

K-Number: K800281 · 1980-03-12

ApplicantMedspec Corp.
Decision Date1980-03-12
Product CodeGDY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MEDSPEC PACKING GAUZE is the device name listed in this FDA 510(k) record. The listed applicant is Medspec Corp.. It received FDA 510(k) clearance on 1980-03-12 under 510(k) number K800281. 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 MEDSPEC PACKING GAUZE?

MEDSPEC PACKING GAUZE is a medical device that received FDA 510(k) clearance on 1980-03-12. The listed applicant is Medspec Corp.. The 510(k) number is K800281.

When did MEDSPEC PACKING GAUZE receive FDA 510(k) clearance?

MEDSPEC PACKING GAUZE received FDA 510(k) clearance on 1980-03-12, under 510(k) number K800281.

Who is the listed applicant for MEDSPEC PACKING GAUZE?

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

What is the FDA product code for MEDSPEC PACKING GAUZE?

The FDA product code for MEDSPEC PACKING GAUZE 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 Medspec 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 15 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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