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FDA 510(k)

RUBBER INFLATABLE RING

K-Number: K823903 · 1983-01-14

ApplicantDuro-Med Ind., Inc.
Decision Date1983-01-14
Product CodeKIC
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

RUBBER INFLATABLE RING is the device name listed in this FDA 510(k) record. The listed applicant is Duro-Med Ind., Inc.. It received FDA 510(k) clearance on 1983-01-14 under 510(k) number K823903. The device is classified under product code KIC. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RUBBER INFLATABLE RING?

RUBBER INFLATABLE RING is a medical device that received FDA 510(k) clearance on 1983-01-14. The listed applicant is Duro-Med Ind., Inc.. The 510(k) number is K823903.

When did RUBBER INFLATABLE RING receive FDA 510(k) clearance?

RUBBER INFLATABLE RING received FDA 510(k) clearance on 1983-01-14, under 510(k) number K823903.

Who is the listed applicant for RUBBER INFLATABLE RING?

The FDA 510(k) record lists Duro-Med Ind., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RUBBER INFLATABLE RING?

The FDA product code for RUBBER INFLATABLE RING is KIC.

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.

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Other records listing Duro-Med Ind., 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.

K803177MOIST HEAT PACK

Related Devices (Code: KIC)

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.

K960189GEL-T CUSHIONSpan-America Medical Systems, Inc.K953352PROTEAM CUSHIONIskra.MedK954117CUSTOMCARE SEATING SYSTEMSpan-America Medical Systems, Inc.K950085MULTICURE(R) S GEL PADMultigestion (Deutschland) GmbHK945667MICOS MICROPULSE(TM) ALTERNATING PRESSURE WHEELCHAIR CUSHIONMicos Medical SystemsK941858GEL CUSHIONHollister, Inc.

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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