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FDA 510(k)

DETECTOR, UV, MOLEL GC-55

K-Number: K770638 · 1977-06-24

ApplicantPeokin-Elmer Corp.
Decision Date1977-06-24
Product CodeKIE
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DETECTOR, UV, MOLEL GC-55 is the device name listed in this FDA 510(k) record. The listed applicant is Peokin-Elmer Corp.. It received FDA 510(k) clearance on 1977-06-24 under 510(k) number K770638. The device is classified under product code KIE. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DETECTOR, UV, MOLEL GC-55?

DETECTOR, UV, MOLEL GC-55 is a medical device that received FDA 510(k) clearance on 1977-06-24. The listed applicant is Peokin-Elmer Corp.. The 510(k) number is K770638.

When did DETECTOR, UV, MOLEL GC-55 receive FDA 510(k) clearance?

DETECTOR, UV, MOLEL GC-55 received FDA 510(k) clearance on 1977-06-24, under 510(k) number K770638.

Who is the listed applicant for DETECTOR, UV, MOLEL GC-55?

The FDA 510(k) record lists Peokin-Elmer Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DETECTOR, UV, MOLEL GC-55?

The FDA product code for DETECTOR, UV, MOLEL GC-55 is KIE.

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 Peokin-Elmer Corp. 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.

K770639DETECTOR, IR, MODEL GC-33

Related Devices (Code: KIE)

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.

K964588WATERS 515 HPLC PUMP (515)Waters CorporationK935666PERKIN-ELMER SERIES 200 LIQ CHROMATOGRAPHIC PUMPThe Perkin-Elmer Corp.K924347WATERS(TM) 996 PDAMillipore Corp.K914841CHROMATOGRAPHY CLINICAL USE 75JQRMillipore Corp.K911299EQUIPMENT/MATERIAL DECONTAMINATING KITRohm and Haas Co.K862506THE WATERS MODEL 990 PHOTODIODE ARRAY DETECTORMillipore Corp.

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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