FDA 510(k)

A-SORB

K-Number: K882115 · 1988-10-03

Decision Date1988-10-03

Product CodeNAB

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

A-SORB is the device name listed in this FDA 510(k) record. The listed applicant is Howard Medical Co.. It received FDA 510(k) clearance on 1988-10-03 under 510(k) number K882115. 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 A-SORB?

A-SORB is a medical device that received FDA 510(k) clearance on 1988-10-03. The listed applicant is Howard Medical Co.. The 510(k) number is K882115.

When did A-SORB receive FDA 510(k) clearance?

A-SORB received FDA 510(k) clearance on 1988-10-03, under 510(k) number K882115.

Who is the listed applicant for A-SORB?

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

What is the FDA product code for A-SORB?

The FDA product code for A-SORB is NAB.

Other records listing Howard Medical 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.

K962234STERILE GAUZE SPONGE - PICK-UPS 12PLY (GS-412), PICK-UPS 16PLY (GS-416)K820195OR SPECIALTIES VAGINAL PACK

Related Devices (Code: NAB)

K946015IVALON EXTERNAL SPONGEIvalon K940755ISOLYER (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.