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FDA 510(k)

WHEELCHAIR BELT

K-Number: K772421 · 1978-01-05

ApplicantFred Sammons, Inc.
Decision Date1978-01-05
Product CodeIQB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

WHEELCHAIR BELT 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 1978-01-05 under 510(k) number K772421. The device is classified under product code IQB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WHEELCHAIR BELT?

WHEELCHAIR BELT is a medical device that received FDA 510(k) clearance on 1978-01-05. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K772421.

When did WHEELCHAIR BELT receive FDA 510(k) clearance?

WHEELCHAIR BELT received FDA 510(k) clearance on 1978-01-05, under 510(k) number K772421.

Who is the listed applicant for WHEELCHAIR BELT?

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 WHEELCHAIR BELT?

The FDA product code for WHEELCHAIR BELT is IQB.

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Other records listing Fred Sammons, 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.

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Related Devices (Code: IQB)

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.

K772420REAR FASTENING SAFETY STRAPFred 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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