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FDA 510(k)

PHOTIC-100 SPECTROPHOTOMETER

K-Number: K854679 · 1986-02-20

ApplicantFuture Impex Corp.
Decision Date1986-02-20
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PHOTIC-100 SPECTROPHOTOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Future Impex Corp.. It received FDA 510(k) clearance on 1986-02-20 under 510(k) number K854679. The device is classified under product code JJQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHOTIC-100 SPECTROPHOTOMETER?

PHOTIC-100 SPECTROPHOTOMETER is a medical device that received FDA 510(k) clearance on 1986-02-20. The listed applicant is Future Impex Corp.. The 510(k) number is K854679.

When did PHOTIC-100 SPECTROPHOTOMETER receive FDA 510(k) clearance?

PHOTIC-100 SPECTROPHOTOMETER received FDA 510(k) clearance on 1986-02-20, under 510(k) number K854679.

Who is the listed applicant for PHOTIC-100 SPECTROPHOTOMETER?

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

What is the FDA product code for PHOTIC-100 SPECTROPHOTOMETER?

The FDA product code for PHOTIC-100 SPECTROPHOTOMETER is JJQ.

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Other records listing Future Impex 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.

K861487ST-90 SPIRO ANALIZERK854686TE-25 COAGURO METERK854687ERMA HB-METER MODEL 303NK854685DIGITAL-9 KEY LEUCOCYTE COUNTERK854677ERMA PC-604 BLOOD CELL COUNTERK854678ERMA PC-602 PC-603 BLOOD CELL COUNTER

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Related Devices (Code: JJQ)

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.

K013371UBIT-IR300 INFRARED SPECTROMETRY SYSTEMOtsuka Pharmaceutical Co., Ltd.K980120DIGENE DML 2000 MICROPLATE LUMINOMETERDigene Corp.K973938ALPHA 4 LS AUTOMATED MICROTITERPLATE PROCESSOR AND READERSfri, Inc.K974762STAT TRACKSAwareness Technology, Inc.K962113ANTHOS PHACTS VERSION MICROPLATE READERColumbia Bioscience, Inc.K961183CBI 7520 READERColumbia Bioscience, 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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