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FDA 510(k)

ELASTO-GEL CAST & SPLINT PADS

K-Number: K872488 · 1987-09-21

ApplicantSouthwest Technologies, Inc.
Decision Date1987-09-21
Product CodeIPM
Advisory CommitteePM
DecisionSubstantially Equivalent for Some Indications

Device Summary

ELASTO-GEL CAST & SPLINT PADS is the device name listed in this FDA 510(k) record. The listed applicant is Southwest Technologies, Inc.. It received FDA 510(k) clearance on 1987-09-21 under 510(k) number K872488. The device is classified under product code IPM. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the ELASTO-GEL CAST & SPLINT PADS?

ELASTO-GEL CAST & SPLINT PADS is a medical device that received FDA 510(k) clearance on 1987-09-21. The listed applicant is Southwest Technologies, Inc.. The 510(k) number is K872488.

When did ELASTO-GEL CAST & SPLINT PADS receive FDA 510(k) clearance?

ELASTO-GEL CAST & SPLINT PADS received FDA 510(k) clearance on 1987-09-21, under 510(k) number K872488.

Who is the listed applicant for ELASTO-GEL CAST & SPLINT PADS?

The FDA 510(k) record lists Southwest Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELASTO-GEL CAST & SPLINT PADS?

The FDA product code for ELASTO-GEL CAST & SPLINT PADS is IPM.

Related Clinical Trials

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Other records listing Southwest Technologies, Inc. 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.

K102478OTC ELASTO-GEL MANUKA HONEY WOUND DRESSINGK083334ELASTO-GEL MANUKA HONEY WOUND DRESSINGK030774STIMULEN COLLAGENK872165ELASTO-GEL OCCLUSIVE DRESSING

Related Devices (Code: IPM)

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.

K823399COVER LIMBOrthopedic Systems, Inc.K801627COVER, LIMBThe Owenby Co.K780905LIMB COVERHydro-Med Products, Inc.K770223HEAVY FOAM HEEL & ELBOW PROTECTORSRobert R. MooreK761114FOAM SLIPPERSFred Sammons, 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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