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FDA 510(k)

BASIN, STERILE (#3200)

K-Number: K760085 · 1976-07-20

ApplicantConcord Laboratories, Inc.
Decision Date1976-07-20
Product CodeFNY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BASIN, STERILE (#3200) is the device name listed in this FDA 510(k) record. The listed applicant is Concord Laboratories, Inc.. It received FDA 510(k) clearance on 1976-07-20 under 510(k) number K760085. The device is classified under product code FNY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BASIN, STERILE (#3200)?

BASIN, STERILE (#3200) is a medical device that received FDA 510(k) clearance on 1976-07-20. The listed applicant is Concord Laboratories, Inc.. The 510(k) number is K760085.

When did BASIN, STERILE (#3200) receive FDA 510(k) clearance?

BASIN, STERILE (#3200) received FDA 510(k) clearance on 1976-07-20, under 510(k) number K760085.

Who is the listed applicant for BASIN, STERILE (#3200)?

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

What is the FDA product code for BASIN, STERILE (#3200)?

The FDA product code for BASIN, STERILE (#3200) is FNY.

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Other records listing Concord Laboratories, 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.

K883840DRI-VENT ARTERIAL BLOOD SAMPLING KITK871825MECONIUM SUCTION CATHETERK864535TRACHEOBRONCHIAL SUCTION CATHETER, CAT. NO. 6110K862039CONCORD CARE TRAYK854601SPRING GUIDE CATHETER ANESTHESIA CONDUCTION CATHK854327SUBCUTANEOUS TUNNELING NEEDLES & HANDLES

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Related Devices (Code: FNY)

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.

K832826AAP DOSIMETRY RELEASE OR BASIN SETSAmerican Hospital Supply Corp.K802538BASIN PACKTexas Medical Products, Inc.K800440STERILE SPONGE BOWLSPremium Plastics, Inc.K792625STERILIZATION PROCESS/PLACENTA BASINProcter & Gamble Mfg. Co.K7717338 EMESIS BASINBemis Health CareK760495BASIN, RECTANGULAR WASHLandmark Plastics

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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