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FDA 510(k)

PARKE-DAVIS NON-WOVEN SPONGE

K-Number: K810318 · 1981-02-26

ApplicantHospital Products Co.
Decision Date1981-02-26
Product CodeNAB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PARKE-DAVIS NON-WOVEN SPONGE is the device name listed in this FDA 510(k) record. The listed applicant is Hospital Products Co.. It received FDA 510(k) clearance on 1981-02-26 under 510(k) number K810318. 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 PARKE-DAVIS NON-WOVEN SPONGE?

PARKE-DAVIS NON-WOVEN SPONGE is a medical device that received FDA 510(k) clearance on 1981-02-26. The listed applicant is Hospital Products Co.. The 510(k) number is K810318.

When did PARKE-DAVIS NON-WOVEN SPONGE receive FDA 510(k) clearance?

PARKE-DAVIS NON-WOVEN SPONGE received FDA 510(k) clearance on 1981-02-26, under 510(k) number K810318.

Who is the listed applicant for PARKE-DAVIS NON-WOVEN SPONGE?

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

What is the FDA product code for PARKE-DAVIS NON-WOVEN SPONGE?

The FDA product code for PARKE-DAVIS NON-WOVEN SPONGE is NAB.

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.

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Other records listing Hospital Products Co. 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.

K823696MICRO Z BLOOD COLLECTING NEEDLESK801602DESERET I.V. FILTERK801173ANGIO-FLO MONITORING KITK792386NUTRA-PH INSTRUMENT MILKK791350POPE AMBULATORY HALO VEST

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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