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FDA 510(k)

GRIP-A-BOOTS

K-Number: K955463 · 1996-01-23

ApplicantSil-Med Corp.
Decision Date1996-01-23
Product CodeLXZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

GRIP-A-BOOTS is the device name listed in this FDA 510(k) record. The listed applicant is Sil-Med Corp.. It received FDA 510(k) clearance on 1996-01-23 under 510(k) number K955463. The device is classified under product code LXZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GRIP-A-BOOTS?

GRIP-A-BOOTS is a medical device that received FDA 510(k) clearance on 1996-01-23. The listed applicant is Sil-Med Corp.. The 510(k) number is K955463.

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

GRIP-A-BOOTS received FDA 510(k) clearance on 1996-01-23, under 510(k) number K955463.

Who is the listed applicant for GRIP-A-BOOTS?

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

What is the FDA product code for GRIP-A-BOOTS?

The FDA product code for GRIP-A-BOOTS is LXZ.

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Other records listing Sil-Med 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.

K972521NAVIGATOR (STYLET) 2006K961392ANTIMICROBIAL PERITONEAL DIALYSIS COIL CATHETER WITH SPI-ARGENT IIK961194ANTIMICROBIAL MEDIASTINAL SILICONE DRAINK961295SAPPHIRE LINE FLAT DRAIN/KIT WITH SPI-ARGENT II W/OR W/OUT TROCARK960099PENROSE DRAIN MODELS 6001 - 6007K942709MEDIASTINAL SILICONE DRAINS

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Related Devices (Code: LXZ)

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.

K834127INSTRUMENT TIP PROTECTION COVERSDevon Industries, 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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