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FDA 510(k)

BLF EIKEN KIT DETER. OF B-LIPOPR. FRAC.

K-Number: K802451 · 1981-01-09

ApplicantSyn-Kit, Inc.
Decision Date1981-01-09
Product CodeJHQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BLF EIKEN KIT DETER. OF B-LIPOPR. FRAC. is the device name listed in this FDA 510(k) record. The listed applicant is Syn-Kit, Inc.. It received FDA 510(k) clearance on 1981-01-09 under 510(k) number K802451. The device is classified under product code JHQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLF EIKEN KIT DETER. OF B-LIPOPR. FRAC.?

BLF EIKEN KIT DETER. OF B-LIPOPR. FRAC. is a medical device that received FDA 510(k) clearance on 1981-01-09. The listed applicant is Syn-Kit, Inc.. The 510(k) number is K802451.

When did BLF EIKEN KIT DETER. OF B-LIPOPR. FRAC. receive FDA 510(k) clearance?

BLF EIKEN KIT DETER. OF B-LIPOPR. FRAC. received FDA 510(k) clearance on 1981-01-09, under 510(k) number K802451.

Who is the listed applicant for BLF EIKEN KIT DETER. OF B-LIPOPR. FRAC.?

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

What is the FDA product code for BLF EIKEN KIT DETER. OF B-LIPOPR. FRAC.?

The FDA product code for BLF EIKEN KIT DETER. OF B-LIPOPR. FRAC. is JHQ.

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Other records listing Syn-Kit, 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.

K861098SEROIDEN STREPTO KIT 'EIKEN'K861631SLIDE CULTURE U 'EIKEN'K854819CPR SLIDE EIKENK854820RA 80 EIKENK853276ASO SLIDE EIKENK843758UROPAPER EIKEN GK

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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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