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FDA 510(k)

ULTRA-PAN FOR ORTHOTIC PLASTICS (7262)

K-Number: K880644 · 1988-05-06

ApplicantFred Sammons, Inc.
Decision Date1988-05-06
Product CodeIRQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ULTRA-PAN FOR ORTHOTIC PLASTICS (7262) 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 1988-05-06 under 510(k) number K880644. The device is classified under product code IRQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRA-PAN FOR ORTHOTIC PLASTICS (7262)?

ULTRA-PAN FOR ORTHOTIC PLASTICS (7262) is a medical device that received FDA 510(k) clearance on 1988-05-06. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K880644.

When did ULTRA-PAN FOR ORTHOTIC PLASTICS (7262) receive FDA 510(k) clearance?

ULTRA-PAN FOR ORTHOTIC PLASTICS (7262) received FDA 510(k) clearance on 1988-05-06, under 510(k) number K880644.

Who is the listed applicant for ULTRA-PAN FOR ORTHOTIC PLASTICS (7262)?

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 ULTRA-PAN FOR ORTHOTIC PLASTICS (7262)?

The FDA product code for ULTRA-PAN FOR ORTHOTIC PLASTICS (7262) is IRQ.

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Other records listing Fred Sammons, Inc. as applicant

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Related Devices (Code: IRQ)

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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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