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FDA 510(k)

CRUTCH & WALKER PADS

K-Number: K811493 · 1981-06-12

ApplicantFred Sammons, Inc.
Decision Date1981-06-12
Product CodeINP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CRUTCH & WALKER PADS is the device name listed in this FDA 510(k) record. The listed applicant is Fred Sammons, Inc.. It received FDA 510(k) clearance on 1981-06-12 under 510(k) number K811493. The device is classified under product code INP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CRUTCH & WALKER PADS?

CRUTCH & WALKER PADS is a medical device that received FDA 510(k) clearance on 1981-06-12. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K811493.

When did CRUTCH & WALKER PADS receive FDA 510(k) clearance?

CRUTCH & WALKER PADS received FDA 510(k) clearance on 1981-06-12, under 510(k) number K811493.

Who is the listed applicant for CRUTCH & WALKER PADS?

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

What is the FDA product code for CRUTCH & WALKER PADS?

The FDA product code for CRUTCH & WALKER PADS is INP.

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Other records listing Fred Sammons, Inc. as applicant

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Related Devices (Code: INP)

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.

K831889SURGEON'S CHOICE CRUTCH HANDLEW.K. Wheeler, Inc.K831149PERSONAL KNEE CRUTCH PADTecnol New Jersey Wound Care, Inc.K810650CRUTCH TIPS & GRIPSFirst Industries, Inc.K803136CONPHAR CRUTCH TIPSConphar, Inc.K803144CONPHAR CRUTCH PADSConphar, Inc.K803140CONPHAR CRUTCH GRIPSConphar, 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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