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FDA 510(k)

POTASSIUM HYDROXIDE W/GLYCEROL MTG FL.

K-Number: K760837 · 1976-11-16

ApplicantI M, Inc.
Decision Date1976-11-16
Product Code
DecisionSubstantially Equivalent

Device Summary

POTASSIUM HYDROXIDE W/GLYCEROL MTG FL. is the device name listed in this FDA 510(k) record. The listed applicant is I M, Inc.. It received FDA 510(k) clearance on 1976-11-16 under 510(k) number K760837. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POTASSIUM HYDROXIDE W/GLYCEROL MTG FL.?

POTASSIUM HYDROXIDE W/GLYCEROL MTG FL. is a medical device that received FDA 510(k) clearance on 1976-11-16. The listed applicant is I M, Inc.. The 510(k) number is K760837.

When did POTASSIUM HYDROXIDE W/GLYCEROL MTG FL. receive FDA 510(k) clearance?

POTASSIUM HYDROXIDE W/GLYCEROL MTG FL. received FDA 510(k) clearance on 1976-11-16, under 510(k) number K760837.

Who is the listed applicant for POTASSIUM HYDROXIDE W/GLYCEROL MTG FL.?

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

Related Clinical Trials

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Other records listing I M, 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.

K914600NEUROLOGICAL SPONGEK892389BIOPSY KITK881363SYRINGE PREFILLED WITH WATERK880753UMBILICAL CORD CLAMPK872741NUTRIPUMPK871495BANDAGES CATALOG NUMBER: 101 TO 220

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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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