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FDA 510(k)

NON-STICK PADS

K-Number: K780549 · 1978-04-19

ApplicantNational Patent Development Corp.
Decision Date1978-04-19
Product CodeNAB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NON-STICK PADS is the device name listed in this FDA 510(k) record. The listed applicant is National Patent Development Corp.. It received FDA 510(k) clearance on 1978-04-19 under 510(k) number K780549. The device is classified under product code NAB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NON-STICK PADS?

NON-STICK PADS is a medical device that received FDA 510(k) clearance on 1978-04-19. The listed applicant is National Patent Development Corp.. The 510(k) number is K780549.

When did NON-STICK PADS receive FDA 510(k) clearance?

NON-STICK PADS received FDA 510(k) clearance on 1978-04-19, under 510(k) number K780549.

Who is the listed applicant for NON-STICK PADS?

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

What is the FDA product code for NON-STICK PADS?

The FDA product code for NON-STICK PADS is NAB.

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Other records listing National Patent Development Corp. as applicant

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Related Devices (Code: NAB)

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.

K946015IVALON EXTERNAL SPONGEIvalonK940755ISOLYER (4X4, 8PLY)Isolyer Co.K931610OMNISORB II, NONWOVEN SPONGE, STERILE AND NONOmni Mfg., Inc.K925590MULTI-TRAUMA DRESSINGGam Industries, Inc.K926072K-BAND AND K-CREPEParema , Ltd.K915591STERILE GAUZE PADSEagle Medical, Inc.

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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