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FDA 510(k)

MUL-T-PAD

K-Number: K760706 · 1976-10-06

ApplicantGaymar Industries, Inc.
Decision Date1976-10-06
Product CodeIMD
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MUL-T-PAD is the device name listed in this FDA 510(k) record. The listed applicant is Gaymar Industries, Inc.. It received FDA 510(k) clearance on 1976-10-06 under 510(k) number K760706. The device is classified under product code IMD. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MUL-T-PAD?

MUL-T-PAD is a medical device that received FDA 510(k) clearance on 1976-10-06. The listed applicant is Gaymar Industries, Inc.. The 510(k) number is K760706.

When did MUL-T-PAD receive FDA 510(k) clearance?

MUL-T-PAD received FDA 510(k) clearance on 1976-10-06, under 510(k) number K760706.

Who is the listed applicant for MUL-T-PAD?

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

What is the FDA product code for MUL-T-PAD?

The FDA product code for MUL-T-PAD is IMD.

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Related Devices (Code: IMD)

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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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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