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FDA 510(k)

CONPHAR O.R. HEAD COVER-STERILE

K-Number: K792106 · 1979-11-05

ApplicantConphar, Inc.
Decision Date1979-11-05
Product CodeFYI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CONPHAR O.R. HEAD COVER-STERILE is the device name listed in this FDA 510(k) record. The listed applicant is Conphar, Inc.. It received FDA 510(k) clearance on 1979-11-05 under 510(k) number K792106. The device is classified under product code FYI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONPHAR O.R. HEAD COVER-STERILE?

CONPHAR O.R. HEAD COVER-STERILE is a medical device that received FDA 510(k) clearance on 1979-11-05. The listed applicant is Conphar, Inc.. The 510(k) number is K792106.

When did CONPHAR O.R. HEAD COVER-STERILE receive FDA 510(k) clearance?

CONPHAR O.R. HEAD COVER-STERILE received FDA 510(k) clearance on 1979-11-05, under 510(k) number K792106.

Who is the listed applicant for CONPHAR O.R. HEAD COVER-STERILE?

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 O.R. HEAD COVER-STERILE?

The FDA product code for CONPHAR O.R. HEAD COVER-STERILE is FYI.

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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: FYI)

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.

K871073OMEGA BIVALVE NASAL SPLINTSOmega Silicone, Inc.K821178ETHICON EXTERNAL FIXATION WIREETHICON, Inc.K801072STRAITH NASAL SPLINTSurgical Technology Laboratories, 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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