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FDA 510(k)

POROUS ELASTIC RUBBER BANDAGE

K-Number: K792065 · 1979-11-20

ApplicantNorman R. Sanborn Co.
Decision Date1979-11-20
Product CodeFQM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

POROUS ELASTIC RUBBER BANDAGE is the device name listed in this FDA 510(k) record. The listed applicant is Norman R. Sanborn Co.. It received FDA 510(k) clearance on 1979-11-20 under 510(k) number K792065. The device is classified under product code FQM. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POROUS ELASTIC RUBBER BANDAGE?

POROUS ELASTIC RUBBER BANDAGE is a medical device that received FDA 510(k) clearance on 1979-11-20. The listed applicant is Norman R. Sanborn Co.. The 510(k) number is K792065.

When did POROUS ELASTIC RUBBER BANDAGE receive FDA 510(k) clearance?

POROUS ELASTIC RUBBER BANDAGE received FDA 510(k) clearance on 1979-11-20, under 510(k) number K792065.

Who is the listed applicant for POROUS ELASTIC RUBBER BANDAGE?

The FDA 510(k) record lists Norman R. Sanborn Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POROUS ELASTIC RUBBER BANDAGE?

The FDA product code for POROUS ELASTIC RUBBER BANDAGE is FQM.

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Related Devices (Code: FQM)

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.

K040936PETIT SILMA ELASTIC BANDAGE WITH GERMANIUM/TITANIUM OXIDELeda Co., Ltd.K040054BACK IN ACTION COMPRESSION & SUPPORT WITH MAGNETS FOR THE LOWER BACK, KNEE AND ANKLETheodore BarashK013244COMFORTCARE COMPRESSION SUPPORT WITIH MAGNETS AND AEGIS MICROBE SHIELD COMFORTCARE MAGNETIC INSOLES AND AEGIS MICROBEMed Gen, Inc.K952738SKIN SAVER SYSTEMSSkin Saver Systems, Inc.K872868ASPEN ESMARK BANDAGEAspen Laboratories, Inc.K840107TUBE-BANDAGE FOR HUMAN DIGITS 200Zens Health Care Products

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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