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FDA 510(k)

MICROPAK MOIST HEAT PAD

K-Number: K830981 · 1983-06-03

Decision Date1983-06-03
Product CodeIME
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MICROPAK MOIST HEAT PAD is the device name listed in this FDA 510(k) record. The listed applicant is Micropak Manufacturers, Inc.. It received FDA 510(k) clearance on 1983-06-03 under 510(k) number K830981. The device is classified under product code IME. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROPAK MOIST HEAT PAD?

MICROPAK MOIST HEAT PAD is a medical device that received FDA 510(k) clearance on 1983-06-03. The listed applicant is Micropak Manufacturers, Inc.. The 510(k) number is K830981.

When did MICROPAK MOIST HEAT PAD receive FDA 510(k) clearance?

MICROPAK MOIST HEAT PAD received FDA 510(k) clearance on 1983-06-03, under 510(k) number K830981.

Who is the listed applicant for MICROPAK MOIST HEAT PAD?

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

What is the FDA product code for MICROPAK MOIST HEAT PAD?

The FDA product code for MICROPAK MOIST HEAT PAD is IME.

Related Clinical Trials

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.

Related Devices (Code: IME)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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