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FDA 510(k)

WALKER/CRUTCH BAG

K-Number: K811485 · 1981-06-16

ApplicantFred Sammons, Inc.
Decision Date1981-06-16
Product CodeITJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

WALKER/CRUTCH BAG 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 1981-06-16 under 510(k) number K811485. The device is classified under product code ITJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WALKER/CRUTCH BAG?

WALKER/CRUTCH BAG is a medical device that received FDA 510(k) clearance on 1981-06-16. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K811485.

When did WALKER/CRUTCH BAG receive FDA 510(k) clearance?

WALKER/CRUTCH BAG received FDA 510(k) clearance on 1981-06-16, under 510(k) number K811485.

Who is the listed applicant for WALKER/CRUTCH BAG?

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 WALKER/CRUTCH BAG?

The FDA product code for WALKER/CRUTCH BAG is ITJ.

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Other records listing Fred Sammons, Inc. as applicant

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Related Devices (Code: ITJ)

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.

K833869CHILD'S WALKERKaye Products, Inc.K833195UMBRELLA WALKERConvaid Products, Inc.K830784WALK N ROLLMeta-MorrisK830848RESI-WALKERLic-OrthionK823105RESI-WALKEROrthion Corp.K821404LIGHT WEIGHT ALUMINUM WALKERManuco Manufacturing Co., 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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