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FDA 510(k)

CONPHAR INVALID RING

K-Number: K803137 · 1981-01-08

ApplicantConphar, Inc.
Decision Date1981-01-08
Product CodeKIC
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CONPHAR INVALID RING is the device name listed in this FDA 510(k) record. The listed applicant is Conphar, Inc.. It received FDA 510(k) clearance on 1981-01-08 under 510(k) number K803137. 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 CONPHAR INVALID RING?

CONPHAR INVALID RING is a medical device that received FDA 510(k) clearance on 1981-01-08. The listed applicant is Conphar, Inc.. The 510(k) number is K803137.

When did CONPHAR INVALID RING receive FDA 510(k) clearance?

CONPHAR INVALID RING received FDA 510(k) clearance on 1981-01-08, under 510(k) number K803137.

Who is the listed applicant for CONPHAR INVALID RING?

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

What is the FDA product code for CONPHAR INVALID RING?

The FDA product code for CONPHAR INVALID RING is KIC.

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Other records listing Conphar, 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.

K821825CONPHAR SILICONE FEEDING TUBEK821295OLSEN HEGAR NEEDLE HOLDERSK821289MAYO-HEGAR NEEDLE HOLDERK821354CONPHAR MAYO HEGAR NEEDLE HOLDERK821298BACKHAUS CLAMP, 3 1/2K821290LITTAUER SCISSORS 5 1/2

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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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